SAMN22624615
External Id
dbGaP
INSDC center name
2021-10-27T22:19:19.727Z
INSDC first public
2023-06-15T00:00:25.077Z
INSDC last update
SRS12155268
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS12155268
SRA accession
NCI_CIDR_PC_RareVariation
biospecimen repository
113730-0224133114
biospecimen repository sample id
phs001524
gap_accession
3
gap_consent_code
CADM
gap_consent_short_name
4798469
gap_sample_id
3814757
gap_subject_id
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
113730-0224133114
submitted sample id
GENP6035
submitted subject id
NCI_CIDR_PC_RareVariation
submitter handle
Sample from a human male participant in the dbGaP study The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation
title