SAMN26858737
External Id
dbGaP
INSDC center name
2022-03-22T02:34:12.930Z
INSDC first public
2023-08-19T02:40:17.973Z
INSDC last update
SRS18129142
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS18129142
SRA accession
DNA
analyte type
LargeRecurrentDeletions
biospecimen repository
BG1027
biospecimen repository sample id
Blood
body site
phs002613
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
4899653
gap_sample_id
3887645
gap_subject_id
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Mendelian
study design
Characterizing Disease-Causing Variants Using Personal Genomes with Large Recurrent Deletions
study name
No
subject is affected
BG1027
submitted sample id
BG1027
submitted subject id
LargeRecurrentDeletions
submitter handle
Non-tumor DNA sample from Blood of a human male participant in the dbGaP study Characterizing Disease-Causing Variants Using Personal Genomes with Large Recurrent Deletions
title