SAMN13396490
External Id
dbGaP
INSDC center name
2019-11-26T21:54:59.483Z
INSDC first public
2024-05-04T04:29:58.890Z
INSDC last update
SRS5856598
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS5856598
SRA accession
DNA
analyte type
NCI_FamilialMelanoma
biospecimen repository
A090131
biospecimen repository sample id
phs001177
gap_accession
1
gap_consent_code
HMB-MDS
gap_consent_short_name
3719095
gap_sample_id
3071095
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
Family/Twin/Trios
study design
Melanoma, Cutaneous Malignant
study disease
Rare Germline Variations in Familial Melanoma
study name
Yes
subject is affected
A090131
submitted sample id
A090131
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