A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3569313



Internal ID18697511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16333575..16362286hg38UCSC Ensembl
Innerchr4:16335198..16363909hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3828712
hg1928712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1465e212
Supporting Variantsessv9770306
Samples401931JL
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)esv3569313
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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