A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697861



Internal ID15434513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63754644..63759796hg38UCSC Ensembl
Innerchr10:65514404..65519556hg19UCSC Ensembl
Innerchr10:65184410..65189562hg18UCSC Ensembl
Innerchr10:65184410..65189562hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg385153
hg195153
hg185153
hg175153
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521236
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697861
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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