A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657190



Internal ID15393842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161032271..161085672hg38UCSC Ensembl
Innerchr4:161953423..162006824hg19UCSC Ensembl
Innerchr4:162172873..162226274hg18UCSC Ensembl
Innerchr4:162311028..162364429hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3853402
hg1953402
hg1853402
hg1753402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515755
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657190
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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