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mtDNA Haplogroup • Maternal Lineage

N9B1

mtDNA Haplogroup N9B1

~14,000 years ago
Northeast Asia (Japanese archipelago)
0 subclades
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Chapter I

The Story

The journey of mtDNA haplogroup N9B1

Origins and Evolution

N9B1 is a subclade of mtDNA haplogroup N9B, itself part of the broader East Asian macro-haplogroup N9. Based on the phylogenetic position of N9B1 beneath N9B and the known time-depth of N9B in the Late Upper Paleolithic, N9B1 most plausibly arose in the terminal Pleistocene or early Holocene (roughly ~14 kya, with uncertainty of a few thousand years). Its emergence is consistent with demographic events tied to island colonization, prolonged insular isolation, and local founder effects in the Japanese archipelago and adjacent northeast Asian coastal regions.

Lineage formation for N9B1 likely reflects the same processes that shaped other Jomon-associated maternal lineages: small effective population sizes, drift in relatively isolated groups, and persistence through the Holocene in populations with limited incoming maternal gene flow until more recent historic periods.

Subclades (if applicable)

As a downstream branch of N9B, N9B1 may itself contain further internal diversity (subclades) identified by additional private mutations in whole-mitochondrial genomes. Published ancient DNA and high-resolution modern mitogenome surveys have sometimes resolved sublineages within N9B-derived clades, but sampling remains sparse compared to continental East Asian haplogroups. Continued mitogenome sequencing of ancient Jomon and modern indigenous groups (Ainu, Ryukyuan) is required to refine the internal topology and age estimates of N9B1 subclades.

Geographical Distribution

N9B1 shows a geographically concentrated distribution centered on the Japanese archipelago with lower frequency and sporadic occurrences in neighboring regions. Highest frequencies and most consistent detections are in:

  • Northern and northeastern Japan (Hokkaido, Tohoku), where Jomon ancestry and continuity signals are strongest.
  • Ryukyu/Okinawa populations and some island groups, where insular persistence and drift have preserved indigenous maternal lineages.
  • Ainu and populations with elevated Jomon-derived ancestry.

Lower-frequency occurrences have been reported in mainland Northeast Asia (Korea, coastal Siberia groups such as Nivkh and Ulchi), scattered Han Chinese and other East Asian populations, and very rare finds in Southeast Asia or farther west that likely reflect later, limited gene flow or analytic artifacts. Ancient DNA detections in Jomon-era remains (several reported instances) support a long-term presence in the archipelago.

Historical and Cultural Significance

The distribution and temporal depth of N9B1 tie the haplogroup to Jomon-period hunter-gatherer populations of the Japanese islands, making it a useful marker for studies of prehistoric insular settlement, maternal continuity, and the genetic distinctiveness of indigenous groups such as the Ainu and some Ryukyuan communities. Because N9B1 is relatively enriched in regions with archaeological evidence for long-term habitation and cultural continuity (e.g., Jomon sites in Hokkaido and Tohoku), it is frequently cited in discussions about the maternal genetic legacy of pre-Neolithic and early Holocene populations of Japan.

N9B1's low frequency outside the archipelago and northeastern coastal fringe indicates limited large-scale female-mediated dispersals involving this lineage after its formation; where it does appear off-island, the occurrences are best interpreted as localized prehistoric contacts, historic movements, or recent admixture.

Conclusion

N9B1 is an informative maternal lineage for reconstructing the population history of the Japanese archipelago and adjacent northeast Asian coastal regions. Its origin in the terminal Pleistocene/early Holocene, association with Jomon-period remains, and persistence in modern indigenous groups make it an important haplogroup for studies of insular hunter-gatherer continuity, founder effects, and the maternal component of East Asian demographic history. Further high-resolution mitogenome sampling of ancient and modern populations will clarify internal branching within N9B1 and refine its chronology and geographic microstructure.

Key Points

  • Origins and Evolution
  • Subclades (if applicable)
  • Geographical Distribution
  • Historical and Cultural Significance
  • Conclusion
Chapter II

Tree & Relationships

Phylogenetic context and subclades

Evolution Path

This haplogroup's evolutionary journey from its earliest ancestor to the present.

Steps Haplogroup Age Estimate Archaeology Era Time Passed Immediate Descendants Tested Modern Descendants Ancient Connections
1 N9B1 Current ~14,000 years ago 🏹 Mesolithic 14,000 years 0 0 0
2 N9B ~18,000 years ago 🏹 Mesolithic 18,000 years 3 0 21
3 N9 ~25,000 years ago 🦴 Paleolithic 25,000 years 1 0 0
4 N ~60,000 years ago 🦴 Paleolithic 60,000 years 15 15,452 13
5 L3 ~70,000 years ago 🦴 Paleolithic 70,000 years 11 17,621 6
6 L ~160,000 years ago 🦴 Paleolithic 160,000 years 7 18,987 5

Subclades (0)

Terminal branch - no known subclades

Siblings (2)

Other branches from the same parent haplogroup

Chapter III

Where in the World

Geographic distribution and modern presence

Place of Origin

Northeast Asia (Japanese archipelago)

Modern Distribution

The populations where mtDNA haplogroup N9B1 is found include:

  1. Japanese populations (notably in Hokkaido, Tohoku, and Ryukyu/Okinawa regions)
  2. Ancient Jomon-era remains from the Japanese archipelago
  3. Ainu and Ryukyuan-related modern groups with elevated indigenous maternal ancestry
  4. Koreans and some Northeast Asian mainland populations (lower frequencies)
  5. Indigenous peoples of the Far East / coastal Siberia (e.g., Nivkh, Ulchi; sporadic occurrences)
  6. Han Chinese and other East Asian populations at low frequencies
  7. Southeast Asian populations (rare and localized occurrences)
  8. Central Asian and West Eurasian occurrences that are generally rare and attributable to later or sparse prehistoric gene flow
  9. Modern urban and mixed populations across East and Southeast Asia due to recent admixture
CHAPTER IV

When in Time

Your haplogroup in the context of human history

~20k years ago

Last Glacial Maximum

Peak of the last ice age, populations isolated

~14k years ago

Haplogroup N9B1

Your mtDNA haplogroup emerged in Northeast Asia (Japanese archipelago)

Northeast Asia (Japanese archipelago)
~10k years ago

Neolithic Revolution

Agriculture begins, settled communities form

~5k years ago

Bronze Age

Metalworking, writing, and early civilizations

~3k years ago

Iron Age

Iron tools, expanded trade networks

~2k years ago

Classical Antiquity

Greek and Roman civilizations flourish

Present

Present Day

Modern era

Your Haplogroup
Historical Era
Chapter IV-B

Linked Cultures

Ancient cultures associated with mtDNA haplogroup N9B1

Cultural Heritage

These ancient cultures have been linked to haplogroup N9B1 based on matching ancient DNA samples from archaeological excavations. The presence of this haplogroup in these cultures provides insights into the migrations and population movements of populations carrying this haplogroup.

Early Jomon Jomon
Culture assignments are based on archaeological context of ancient DNA samples and may represent regional associations during specific time periods.
Chapter V

Sample Catalog

Top 50 ancient DNA samples directly related to haplogroup N9B1 or parent clades

50 / 50 samples
Portrait Sample Country Era Date Culture mtDNA Match
Portrait of ancient individual C391 from China, dated 1 CE - 400 CE
C391
China Historical Period Hetian, Xinjiang, China 1 CE - 400 CE Hetian Culture N Direct
Portrait of ancient individual ZLNR-1 from China, dated 81 CE - 236 CE
ZLNR-1
China Iron Age China 81 CE - 236 CE Chinese Iron Age N9a9 Direct
Portrait of ancient individual ZLNR-1 from China, dated 81 CE - 236 CE
ZLNR-1
China Iron Age China 81 CE - 236 CE N9a9 Direct
Portrait of ancient individual I16584 from Turkey, dated 100 BCE - 200 CE
I16584
Turkey Roman Period 2 Turkey 100 BCE - 200 CE Middle Roman Anatolia N1a1b1 Direct
Portrait of ancient individual PCA0480 from Poland, dated 100 CE - 300 CE
PCA0480
Poland Wielbark Culture 100 CE - 300 CE Wielbark N1b1b Direct
Portrait of ancient individual DA39 from Mongolia, dated 150 BCE - 125 CE
DA39
Mongolia Xiongnu Period Mongolia 150 BCE - 125 CE Xiongnu Culture N9a2'4'5'11 Direct
Portrait of ancient individual DA39 from Mongolia, dated 150 BCE - 125 CE
DA39
Mongolia The Xiongnu Empire 150 BCE - 125 CE N9a2'4'5'11 Direct
Portrait of ancient individual SFI-11 from Lebanon, dated 151 BCE - 62 CE
SFI-11
Lebanon Early Roman Lebanon 151 BCE - 62 CE Early Roman Lebanese N1b1 Direct
Portrait of ancient individual SFI-11 from Lebanon, dated 151 BCE - 62 CE
SFI-11
Lebanon Roman Levant 151 BCE - 62 CE N1b1 Direct
Portrait of ancient individual IMA008 from Russia, dated 200 BCE - 100 CE
IMA008
Russia Xiongnu Period Buryatia, Russia 200 BCE - 100 CE Xiongnu Buryat N9a Direct
Chapter VI

Carrier Distribution Map

Geographic distribution of 100 ancient DNA samples carrying haplogroup N9B1

Time Period Filter
All Time Periods
Showing all samples
Each marker represents an ancient individual
Chapter VII

Temporal Distribution

Distribution of carriers across archaeological periods

Chapter VIII

Geographic Distribution

Distribution of carriers by country of origin

Chapter IX

Country × Era Distribution

Cross-tabulation of carrier countries and archaeological periods

Data

Data & Provenance

Source information and data quality

Last Updated 2026-02-16
Confidence Score 50/100
Coverage Low
Data Source

We use the latest phylotree for MTDNA haplogroup classification and data.