A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704167



Internal ID15440819
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 StatusS
Merged Variantsnsv527691
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704167
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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