A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527729



Internal ID15455022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67280304..67473585hg38UCSC Ensembl
Innerchr13:67854436..68047717hg19UCSC Ensembl
Innerchr13:66752437..66945718hg18UCSC Ensembl
Innerchr13:66752437..66945718hg17UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38193282
hg19193282
hg18193282
hg17193282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704211
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527729
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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