A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527691



Internal ID15454984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163355745..163373956hg38UCSC Ensembl
Innerchr4:164276897..164295108hg19UCSC Ensembl
Innerchr4:164496347..164514558hg18UCSC Ensembl
Innerchr4:164634502..164652713hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3818212
hg1918212
hg1818212
hg1718212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704167
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527691
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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