A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520299



Internal ID15100906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73973249..73983709hg38UCSC Ensembl
Innerchr11:73684294..73694754hg19UCSC Ensembl
Innerchr11:73361942..73372402hg18UCSC Ensembl
Innerchr11:73361942..73372402hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810461
hg1910461
hg1810461
hg1710461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662587, nssv662745
Samples
Known GenesUCP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520299
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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