SAMN22624617
External Id
dbGaP
INSDC center name
2021-10-27T22:19:19.803Z
INSDC first public
2023-06-15T00:00:25.673Z
INSDC last update
SRS12156404
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS12156404
SRA accession
DNA
analyte type
NCI_CIDR_PC_RareVariation
biospecimen repository
131525-0238183148
biospecimen repository sample id
Blood
body site
phs001524
gap_accession
2
gap_consent_code
DS-PC-MDS
gap_consent_short_name
4799249
gap_sample_id
3817761
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
Case Set
study design
Prostatic Neoplasms
study disease
The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation
study name
Yes
subject is affected
131525-0238183148
submitted sample id
ICR_5051
submitted subject id
NCI_CIDR_PC_RareVariation
submitter handle
Non-tumor DNA sample from Blood of a human male participant in the dbGaP study The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation
title