A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679534



Internal ID15416186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20501155..20542667hg38UCSC Ensembl
Innerchr10:20790084..20831596hg19UCSC Ensembl
Innerchr10:20830090..20871602hg18UCSC Ensembl
Innerchr10:20830090..20871602hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3841513
hg1941513
hg1841513
hg1741513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516763
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679534
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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