A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698962



Internal ID15435614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118801584..118827753hg38UCSC Ensembl
Innerchr10:120561096..120587265hg19UCSC Ensembl
Innerchr10:120551086..120577255hg18UCSC Ensembl
Innerchr10:120551086..120577255hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3826170
hg1926170
hg1826170
hg1726170
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523236
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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