SAMN07617163
External Id
dbGaP
INSDC center name
2017-09-07T15:52:13.870Z
INSDC first public
2024-05-06T14:09:51.810Z
INSDC last update
SRS2568021
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS2568021
SRA accession
DNA
analyte type
UDN
biospecimen repository
376224e1-b92f-4dd3-b4e0-ccd6fd7f2ee2
biospecimen repository sample id
Blood
body site
phs001232
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
2608203
gap_sample_id
2181342
gap_subject_id
SNP/CNV Genotypes (NGS)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Prospective Longitudinal Cohort
study design
Rare Diseases
study disease
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
study name
Yes
subject is affected
376224e1-b92f-4dd3-b4e0-ccd6fd7f2ee2
submitted sample id
79057e78-c51d-492a-8cf7-fae4161d1e64
submitted subject id
UDN
submitter handle
DNA sample from Blood of a human female participant in the dbGaP study Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
title