A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519282



Internal ID15446575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110691541..110708238hg38UCSC Ensembl
Innerchr13:111343888..111360585hg19UCSC Ensembl
Innerchr13:110141889..110158586hg18UCSC Ensembl
Innerchr13:110141889..110158586hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3816698
hg1916698
hg1816698
hg1716698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696764
Samples
Known GenesCARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519282
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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