A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685791



Internal ID15422443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79955982..79980164hg38UCSC Ensembl
Innerchr10:81715738..81739920hg19UCSC Ensembl
Innerchr10:81705718..81729900hg18UCSC Ensembl
Innerchr10:81705718..81729900hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3824183
hg1924183
hg1824183
hg1724183
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520754
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685791
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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