A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3568702



Internal ID18696900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39157560..39179386hg38UCSC Ensembl
Innerchr3:39199051..39220877hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3821827
hg1921827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766728, essv9766727
Samples400582WS, 402073LQ
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)esv3568702
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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