A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3571308



Internal ID18352820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:96954080..96960315hg38UCSC Ensembl
Innerchr6:97401956..97408191hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386236
hg196236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9780981, essv9780980, essv9780983, essv9780985, essv9780982, essv9780984
Samples401030GI, 400749VW, 400341GL, 401939GD, 400668TD, 400704LC
Known GenesKLHL32
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)esv3571308
Frequency
Sample Size873
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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