A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700917



Internal ID15090883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71520942..71525704hg38UCSC Ensembl
Innerchr10:73280699..73285461hg19UCSC Ensembl
Innerchr10:72950705..72955467hg18UCSC Ensembl
Innerchr10:72950705..72955467hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384763
hg194763
hg184763
hg174763
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524906
Supporting Variants
Samples
Known GenesCDH23
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700917
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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