A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521889



Internal ID15449182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:106127748..106128909hg38UCSC Ensembl
Innerchr13:106780097..106781258hg19UCSC Ensembl
Innerchr13:105578098..105579259hg18UCSC Ensembl
Innerchr13:105578098..105579259hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381162
hg191162
hg181162
hg171162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694661
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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