SAMN00009202
EXTERNALSample
- Accession
SAMN00009202- Alias
- HG01248
- Sex
- Female
- Center
- NYGC
- Description
- Human 1000 genomes individual HG01248
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
chrM:5672G>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
-
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
-
MchrM:14206T>C, chrM:14466G>A, chrM:16482T>C, chrM:9823C>T
-
CZchrM:14910A>T, chrM:15721T>C, chrM:4138A>G, chrM:6619C>A, chrM:8007G>A
-
C1chrM:11337G>A, chrM:12686A>G, chrM:13741T>C, chrM:15748T>C, chrM:2975T>A, chrM:8968A>G
-
C1dchrM:15474A>G
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chrM:5672G>AchrM:10932C>T, chrM:13182G>A, chrM:14804C>T, chrM:15758A>G, chrM:5672G>A, chrM:7053T>C, chrM:8048C>A
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 993300908 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG01248.final.cram | CRAM | — | GRCh38 | bwa mem | d7ef53545ef854e6427bc8581cf91ee1 | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.