A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687793



Internal ID15424445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:124625564..124636239hg38UCSC Ensembl
Innerchr5:123961257..123971932hg19UCSC Ensembl
Innerchr5:123989156..123999831hg18UCSC Ensembl
Innerchr5:123989156..123999831hg17UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3810676
hg1910676
hg1810676
hg1710676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519664
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687793
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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