A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520993



Internal ID15448286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99163130..99219777hg38UCSC Ensembl
Innerchr11:99033861..99090508hg19UCSC Ensembl
Innerchr11:98539071..98595718hg18UCSC Ensembl
Innerchr11:98539071..98595718hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3856648
hg1956648
hg1856648
hg1756648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697726
Samples
Known GenesCNTN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520993
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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