A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524489



Internal ID15105096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71532667..71533031hg38UCSC Ensembl
Innerchr10:73292424..73292788hg19UCSC Ensembl
Innerchr10:72962430..72962794hg18UCSC Ensembl
Innerchr10:72962430..72962794hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38365
hg19365
hg18365
hg17365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700427
Samples
Known GenesCDH23
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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