A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697528



Internal ID15434180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167899070..167910199hg38UCSC Ensembl
Innerchr4:168820221..168831350hg19UCSC Ensembl
Innerchr4:169056796..169067925hg18UCSC Ensembl
Innerchr4:169194951..169206080hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3811130
hg1911130
hg1811130
hg1711130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515790
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697528
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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