A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519664



Internal ID15446957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:124625564..124636285hg38UCSC Ensembl
Innerchr5:123961257..123971978hg19UCSC Ensembl
Innerchr5:123989156..123999877hg18UCSC Ensembl
Innerchr5:123989156..123999877hg17UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3810722
hg1910722
hg1810722
hg1710722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657460, nssv687793
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519664
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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