A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583341



Internal ID18364853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29817304..29821967hg38UCSC Ensembl
Innerchr19:30308211..30312874hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384664
hg194664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1035e212
Supporting Variantsessv9817305
Samples401477ST
Known GenesCCNE1
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)esv3583341
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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