A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583887



Internal ID18712085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79147050..79168003hg38UCSC Ensembl
Innerchr2:79374176..79395129hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3820954
hg1920954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1135e212
Supporting Variantsessv9828155
Samples401016IT
Known GenesREG3A
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3583887
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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