A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697261



Internal ID15433913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65576927..65584951hg38UCSC Ensembl
Innerchr10:67336685..67344709hg19UCSC Ensembl
Innerchr10:67006691..67014715hg18UCSC Ensembl
Innerchr10:67006691..67014715hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg388025
hg198025
hg188025
hg178025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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