A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695387



Internal ID15432039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15286448..15534072hg38UCSC Ensembl
Innerchr9:15286446..15534070hg19UCSC Ensembl
Innerchr9:15276446..15524070hg18UCSC Ensembl
Innerchr9:15276446..15524070hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38247625
hg19247625
hg18247625
hg17247625
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517975
Supporting Variants
Samples
Known GenesPSIP1, SNAPC3, TTC39B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695387
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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