SAMN13396249
External Id
dbGaP
INSDC center name
2019-11-26T21:54:47.313Z
INSDC first public
2024-05-05T12:35:26.670Z
INSDC last update
SRS5853483
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS5853483
SRA accession
DNA
analyte type
NCI_FamilialMelanoma
biospecimen repository
X311605745
biospecimen repository sample id
phs001177
gap_accession
1
gap_consent_code
HMB-MDS
gap_consent_short_name
3721719
gap_sample_id
3073631
gap_subject_id
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
sex
Family/Twin/Trios
study design
Rare Germline Variations in Familial Melanoma
study name
No
subject is affected
X311605745
submitted sample id
X311605745
submitted subject id
NCI_FamilialMelanoma
submitter handle
Non-tumor DNA sample from Unknown of a human male participant in the dbGaP study Rare Germline Variations in Familial Melanoma
title