A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523586



Internal ID15450879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:87044070..87055061hg38UCSC Ensembl
Innerchr5:86339887..86350878hg19UCSC Ensembl
Innerchr5:86375643..86386634hg18UCSC Ensembl
Innerchr5:86375643..86386634hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3810992
hg1910992
hg1810992
hg1710992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699376
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523586
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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