A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520687



Internal ID15447980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105193251..105202089hg38UCSC Ensembl
Innerchr13:105845602..105854440hg19UCSC Ensembl
Innerchr13:104643603..104652441hg18UCSC Ensembl
Innerchr13:104643603..104652441hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg388839
hg198839
hg188839
hg178839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674081, nssv679274
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520687
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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