SAMN00262993
EXTERNALSample
- Accession
SAMN00262993- Alias
- HG01894
- Sex
- Female
- Center
- NYGC
- Description
- Human 1000 genomes individual HG01894
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
L3d3b
From de-novo tree placement
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L1'2'3'4'5'6'7chrM:16181G>A
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L2'3'4'5'6'7chrM:12528G>A, chrM:15734C>T, chrM:16187C>T, chrM:2182A>G, chrM:2309C>T, chrM:6569G>A, chrM:7891T>C
-
L2'3'4'6chrM:10111A>G, chrM:10233C>T, chrM:12929T>C, chrM:14724G>A, chrM:15610T>C, chrM:249A>T, chrM:8078T>C
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L3'4chrM:13073T>C, chrM:15701T>C, chrM:16174T>C, chrM:3017T>C, chrM:3527G>A, chrM:6679T>C, chrM:6944A>G
-
L3chrM:193A>G, chrM:442A>G
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chrM:12528A>GchrM:12528A>G, chrM:15547T>C
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L3d1'2'3'4'5'6chrM:13309T>C, chrM:13707C>T, chrM:345T>C, chrM:4570G>A, chrM:6847A>G, chrM:8041T>C
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L3d3chrM:1143G>A, chrM:14484A>G, chrM:4111T>C
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L3d3bchrM:11202C>T, chrM:11469A>T, chrM:13175T>C, chrM:15498T>C, chrM:16145A>G, chrM:6145G>A, chrM:6812T>C, chrM:817G>A, chrM:9175C>T
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 958141786 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG01894.final.cram | CRAM | — | GRCh38 | bwa mem | 268f2453d69cf9a4ac7bfd802c2eefd0 | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.