A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663259



Internal ID15399911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110447119..110463528hg38UCSC Ensembl
Innerchr10:112206877..112223286hg19UCSC Ensembl
Innerchr10:112196867..112213276hg18UCSC Ensembl
Innerchr10:112196867..112213276hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3816410
hg1916410
hg1816410
hg1716410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520369
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663259
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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