A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520669



Internal ID15447962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128312626..128317488hg38UCSC Ensembl
Innerchr11:128182521..128187383hg19UCSC Ensembl
Innerchr11:127687731..127692593hg18UCSC Ensembl
Innerchr11:127687731..127692593hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384863
hg194863
hg184863
hg174863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697548
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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