A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668599



Internal ID15405251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:126069536..126076264hg38UCSC Ensembl
Innerchr5:125405229..125411957hg19UCSC Ensembl
Innerchr5:125433128..125439856hg18UCSC Ensembl
Innerchr5:125433128..125439856hg17UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg386729
hg196729
hg186729
hg176729
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515933
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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