SAMN01905997
External Id
dbGaP
INSDC center name
2013-01-26T01:28:22.767Z
INSDC first public
2024-05-03T22:08:06.497Z
INSDC last update
SRS449754
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS449754
SRA accession
DNA
analyte type
Rare_Pediatric_Phenotypes
biospecimen repository
S7
biospecimen repository sample id
Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs000553
gap_accession
1
gap_consent_code
GRU-MDS
gap_consent_short_name
915370
gap_sample_id
706663
gap_subject_id
Whole blood leukocytes
histological type
No
is tumor
SNP Genotypes (Array)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
Family/Twin/Trios
study design
Familial Exome Sequencing in Rare Pediatric Phenotypes
study name
S7
submitted sample id
x7
submitted subject id
Rare_Pediatric_Phenotypes
submitter handle
Non-tumor DNA sample from Blood of a human participant in the dbGaP study Familial Exome Sequencing in Rare Pediatric Phenotypes
title