A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699257



Internal ID15435909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19686001..19752217hg38UCSC Ensembl
Innerchr10:19974930..20041146hg19UCSC Ensembl
Innerchr10:20014936..20081152hg18UCSC Ensembl
Innerchr10:20014936..20081152hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3866217
hg1966217
hg1866217
hg1766217
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523490
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699257
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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