A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3576540



Internal ID18704738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38640453..38661915hg38UCSC Ensembl
Innerchr8:38497971..38519433hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3821463
hg1921463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9787838
Samples400641WJ
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)esv3576540
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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