A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520637



Internal ID15447930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105176275..105185548hg38UCSC Ensembl
Innerchr13:105828626..105837899hg19UCSC Ensembl
Innerchr13:104626627..104635900hg18UCSC Ensembl
Innerchr13:104626627..104635900hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg389274
hg199274
hg189274
hg179274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697531
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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