SAMN13396039
External Id
dbGaP
INSDC center name
2019-11-26T21:54:37.030Z
INSDC first public
2024-05-08T13:08:43.527Z
INSDC last update
SRS5856037
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS5856037
SRA accession
DNA
analyte type
NCI_FamilialMelanoma
biospecimen repository
X119820454
biospecimen repository sample id
phs001177
gap_accession
1
gap_consent_code
HMB-MDS
gap_consent_short_name
3721177
gap_sample_id
3073089
gap_subject_id
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
sex
Family/Twin/Trios
study design
Rare Germline Variations in Familial Melanoma
study name
No
subject is affected
X119820454
submitted sample id
X119820454
submitted subject id
NCI_FamilialMelanoma
submitter handle
Non-tumor DNA sample from Unknown of a human female participant in the dbGaP study Rare Germline Variations in Familial Melanoma
title