SAMN13395986
External Id
dbGaP
INSDC center name
2019-11-26T21:54:34.500Z
INSDC first public
2024-05-08T13:08:25.693Z
INSDC last update
SRS5853378
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS5853378
SRA accession
DNA
analyte type
NCI_FamilialMelanoma
biospecimen repository
CMM_SUBJECT_001_000002
biospecimen repository sample id
Peripheral Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs001177
gap_accession
1
gap_consent_code
HMB-MDS
gap_consent_short_name
3719746
gap_sample_id
1675578
gap_subject_id
Whole Blood
http://purl.obolibrary.org/obo/UBERON_0000178
histological type
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Family/Twin/Trios
study design
Melanoma, Cutaneous Malignant
study disease
Rare Germline Variations in Familial Melanoma
study name
Yes
subject is affected
CMM_SUBJECT_001_000002
submitted sample id
CMM_SUBJECT_001_000002
submitted subject id
NCI_FamilialMelanoma
submitter handle
Non-tumor DNA sample from Peripheral Blood of a human female participant in the dbGaP study Rare Germline Variations in Familial Melanoma
title