A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521935



Internal ID15449228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:741956..756332hg38UCSC Ensembl
Innerchr10:787896..802272hg19UCSC Ensembl
Innerchr10:777896..792272hg18UCSC Ensembl
Innerchr10:777896..792272hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3814377
hg1914377
hg1814377
hg1714377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n21
Supporting Variantsnssv694704
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521935
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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