SAMN00262972
EXTERNALSample
- Accession
SAMN00262972- Alias
- HG01958
- Sex
- Female
- Center
- NYGC
- Description
- Human 1000 genomes individual HG01958
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
chrM:10635C>T
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
-
L2achrM:6598T>C
-
L2a1'2'3'4chrM:11337G>A, chrM:13226A>G, chrM:13989A>G, chrM:15717C>T, chrM:6697C>T, chrM:7194A>G
-
L2a1chrM:15207T>C, chrM:16174T>C
-
L2a1e1chrM:14022A>G, chrM:2918C>A, chrM:7964G>A, chrM:8213G>A
-
chrM:10635C>TchrM:10635C>T, chrM:15549T>C, chrM:15717C>T, chrM:16135G>A, chrM:16138T>C
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 759652932 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG01958.final.cram | CRAM | — | GRCh38 | bwa mem | ff856be07dd2a0a7401d3a13465cb5cd | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.