A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520272



Internal ID15447565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76326007..76329486hg38UCSC Ensembl
Innerchr13:76900143..76903622hg19UCSC Ensembl
Innerchr13:75798144..75801623hg18UCSC Ensembl
Innerchr13:75798144..75801623hg17UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg383480
hg193480
hg183480
hg173480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697318
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520272
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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