A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526419



Internal ID15453712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:165248235..165328168hg38UCSC Ensembl
Innerchr5:164675241..164755174hg19UCSC Ensembl
Innerchr5:164607819..164687752hg18UCSC Ensembl
Innerchr5:164607819..164687752hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3879934
hg1979934
hg1879934
hg1779934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702720
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526419
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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