SAMN22624928
External Id
dbGaP
INSDC center name
2021-10-27T22:19:34.680Z
INSDC first public
2023-06-15T00:02:20.390Z
INSDC last update
SRS12163657
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS12163657
SRA accession
DNA
analyte type
NCI_CIDR_PC_RareVariation
biospecimen repository
98714-0196323712
biospecimen repository sample id
Blood
body site
phs001524
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
4808082
gap_sample_id
3823083
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
98714-0196323712
submitted sample id
Y01419
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