SAMN07617197
External Id
dbGaP
INSDC center name
2017-09-07T15:52:15.020Z
INSDC first public
2024-05-06T14:10:04.687Z
INSDC last update
SRS2558895
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS2558895
SRA accession
DNA
analyte type
UDN
biospecimen repository
2fe1958d-528a-4633-96f6-b48ed1f5247f
biospecimen repository sample id
Blood
body site
phs001232
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
2608195
gap_sample_id
2181293
gap_subject_id
SNP/CNV Genotypes (NGS)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
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
2fe1958d-528a-4633-96f6-b48ed1f5247f
submitted sample id
59871f71-b81a-4b91-9f57-d6ab12b3a7b4
submitted subject id
UDN
submitter handle
DNA sample from Blood of a human male participant in the dbGaP study Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
title