A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705484



Internal ID15442136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59276464..59321999hg38UCSC Ensembl
Innerchr3:59262190..59307725hg19UCSC Ensembl
Innerchr3:59237230..59282765hg18UCSC Ensembl
Innerchr3:59237230..59282765hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3845536
hg1945536
hg1845536
hg1745536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528810
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705484
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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