SAMN29174495
External Id
dbGaP
INSDC center name
2022-06-17T09:55:13.173Z
INSDC first public
2022-12-24T02:37:15.807Z
INSDC last update
SRS15512663
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS15512663
SRA accession
DNA
analyte type
NIMH_Autism_KCNC2
biospecimen repository
PB.100.p2
biospecimen repository sample id
peripheral blood
body site
phs002698
gap_accession
1
gap_consent_code
GRU-IRB
gap_consent_short_name
5050326
gap_sample_id
4050549
gap_subject_id
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
sex
Family/Twin/Trios
study design
Autism Spectrum Disorder
study disease
Identification of Structural Variants Relevant to Autism by Pacific Biosciences HiFi Whole-Genome Sequencing
study name
Yes
subject is affected
PB.100.p2
submitted sample id
PB.100.p2
submitted subject id
NIMH_Autism_KCNC2
submitter handle
Non-tumor DNA sample from peripheral blood of a human female participant in the dbGaP study Identification of Structural Variants Relevant to Autism by Pacific Biosciences HiFi Whole-Genome Sequencing
title