A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520163



Internal ID15100770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183844488..183858812hg38UCSC Ensembl
Innerchr3:183562276..183576600hg19UCSC Ensembl
Innerchr3:185044970..185059294hg18UCSC Ensembl
Innerchr3:185044978..185059302hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3814325
hg1914325
hg1814325
hg1714325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697257
Samples
Known GenesPARL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520163
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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