A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583082



Internal ID18364594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22058619..22490838hg38UCSC Ensembl
Innerchr14:22526881..22959826hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38432220
hg19432946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv594e212
Supporting Variantsessv9804717
Samples401262RR
Known Genes
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)esv3583082
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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