A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520353



Internal ID15447646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98490429..98526290hg38UCSC Ensembl
Innerchr10:100250186..100286047hg19UCSC Ensembl
Innerchr10:100240176..100276037hg18UCSC Ensembl
Innerchr10:100240176..100276037hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3835862
hg1935862
hg1835862
hg1735862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697368
Samples
Known GenesHPSE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520353
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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