A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3575562



Internal ID18703760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35759275..35907958hg38UCSC Ensembl
Innerchr3:35800767..35949450hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38148684
hg19148684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1367e212
Supporting Variantsessv9837746
Samples401884WJ
Known GenesARPP21
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)esv3575562
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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