SAMN03577904
External Id
dbGaP
INSDC center name
2015-05-01T00:30:27.967Z
INSDC first public
2024-04-19T07:35:36.317Z
INSDC last update
SRS1046814
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS1046814
SRA accession
DNA
analyte type
NHGRI_Ciliopathies_Exome
biospecimen repository
8055899485
biospecimen repository sample id
whole blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs000288
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
1550088
gap_sample_id
1195927
gap_subject_id
whole blood
http://purl.obolibrary.org/obo/UBERON_0000178
histological type
No
is tumor
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
Case-Control
study design
Congenital Abnormalities
study disease
Ciliopathies Exome Sequencing Initiative
study name
Yes
subject is affected
8055899485
submitted sample id
8055899485
submitted subject id
NHGRI_Ciliopathies_Exome
submitter handle
Non-tumor DNA sample from whole blood of a human female participant in the dbGaP study Ciliopathies Exome Sequencing Initiative
title