A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3569623



Internal ID18697821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98591004..98602930hg38UCSC Ensembl
Innerchr4:99512155..99524081hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3811927
hg1911927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1516e212
Supporting Variantsessv9772265, essv9772266, essv9772263, essv9772261, essv9772262, essv9772268, essv9772264
Samples401292ER, 401079HJ, 401457WK, 400615RI, 401210PB, 400769SL, 400255CD
Known GenesTSPAN5
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)esv3569623
Frequency
Sample Size873
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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