A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522616



Internal ID15449909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116390094..116408818hg38UCSC Ensembl
Innerchr5:115725791..115744515hg19UCSC Ensembl
Innerchr5:115753690..115772414hg18UCSC Ensembl
Innerchr5:115753690..115772414hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3818725
hg1918725
hg1818725
hg1718725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706012
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522616
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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