A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524084



Internal ID15451377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163482710..163497780hg38UCSC Ensembl
Innerchr5:162909716..162924786hg19UCSC Ensembl
Innerchr5:162842294..162857364hg18UCSC Ensembl
Innerchr5:162842294..162857364hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3815071
hg1915071
hg1815071
hg1715071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699953
Samples
Known GenesHMMR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524084
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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