SAMN01905998
External Id
dbGaP
INSDC center name
2013-01-26T01:28:23.240Z
INSDC first public
2024-05-03T22:08:06.747Z
INSDC last update
SRS449761
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS449761
SRA accession
DNA
analyte type
Rare_Pediatric_Phenotypes
biospecimen repository
S6
biospecimen repository sample id
Sperm
http://purl.obolibrary.org/obo/CL_0000019
body site
phs000553
gap_accession
1
gap_consent_code
GRU-MDS
gap_consent_short_name
915369
gap_sample_id
706662
gap_subject_id
Gametes
histological type
No
is tumor
SNP Genotypes (Array)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Family/Twin/Trios
study design
Familial Exome Sequencing in Rare Pediatric Phenotypes
study name
No
subject is affected
S6
submitted sample id
x5
submitted subject id
Rare_Pediatric_Phenotypes
submitter handle
Non-tumor DNA sample from Sperm of a human male participant in the dbGaP study Familial Exome Sequencing in Rare Pediatric Phenotypes
title