A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697973



Internal ID15434625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14566408..14691899hg38UCSC Ensembl
Innerchr9:14566406..14691897hg19UCSC Ensembl
Innerchr9:14556406..14681897hg18UCSC Ensembl
Innerchr9:14556406..14681897hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38125492
hg19125492
hg18125492
hg17125492
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521363
Supporting Variants
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697973
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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