A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3582284



Internal ID18363796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70141960..70163851hg38UCSC Ensembl
Innerchr16:70175863..70197754hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3821892
hg1921892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv850e212
Supporting Variantsessv9811218, essv9811217, essv9811216, essv9811220, essv9811219, essv9811221
Samples400920MK, 400204SC, 401214BJ, 401952UH, 401795SP, 401453OL
Known GenesPDPR
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)esv3582284
Frequency
Sample Size873
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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