A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693990



Internal ID15430642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23078403..23087927hg38UCSC Ensembl
Innerchr9:23078402..23087926hg19UCSC Ensembl
Innerchr9:23068402..23077926hg18UCSC Ensembl
Innerchr9:23068402..23077926hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389525
hg199525
hg189525
hg179525
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693990
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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