A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693976



Internal ID15083942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96780046..96789355hg38UCSC Ensembl
Innerchr9:99542328..99551637hg19UCSC Ensembl
Innerchr9:98582149..98591458hg18UCSC Ensembl
Innerchr9:96621883..96631192hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389310
hg199310
hg189310
hg179310
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520001
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693976
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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