A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701274



Internal ID15437926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131441214..131441500hg38UCSC Ensembl
Innerchr10:133239477..133239763hg19UCSC Ensembl
Innerchr10:133129467..133129753hg18UCSC Ensembl
Innerchr10:133129467..133129753hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38287
hg19287
hg18287
hg17287
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516804
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701274
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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