SAMN00779976
EXTERNALSample
- Accession
SAMN00779976- Alias
- HG02667
- Sex
- Female
- Center
- NYGC
- Description
- Human 1000 genomes individual HG02667
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
chrM:13131G>A
From de-novo tree placement
-
L1'2'3'4'5'6'7chrM:16181G>A
-
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
-
L2chrM:12194G>A, chrM:13013G>A, chrM:15813G>A, chrM:16138T>C, chrM:16187T>C, chrM:1840T>C, chrM:7629G>A, chrM:8644A>G, chrM:9538T>C
-
L2a'b'c'dchrM:11367T>C
-
L2b'c'dchrM:16142C>T, chrM:1756C>T
-
L2b'cchrM:14533G>A, chrM:14640G>A, chrM:15942C>T, chrM:16190C>T, chrM:7047T>A, chrM:866G>A
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L2cchrM:104T>C, chrM:13351G>C, chrM:13381G>C, chrM:133G>A, chrM:15272C>T, chrM:16318C>T, chrM:2623T>A
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L2c5chrM:4019G>A
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chrM:4774A>GchrM:13742T>C, chrM:4774A>G
-
chrM:13131G>AchrM:13131G>A, chrM:14129A>G, chrM:15743C>T
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 730240498 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG02667.final.cram | CRAM | — | GRCh38 | bwa mem | 36c12b23b8ee85c1b4a41c64af6f8eb3 | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.