A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3569492



Internal ID18697690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68570171..68676177hg38UCSC Ensembl
Innerchr4:69435889..69541895hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38106007
hg19106007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1496e212
Supporting Variantsessv9771465
Samples401448BJ
Known GenesUGT2B15
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)esv3569492
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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