A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3569284



Internal ID18350796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9858264..9863405hg38UCSC Ensembl
Innerchr4:9859888..9865029hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg385142
hg195142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9770066
Samples401039PA
Known GenesSLC2A9
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)esv3569284
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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