A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1241e212



Internal ID20149697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31449078..31464854hg38UCSC Ensembl
chr20:30036881..30052657hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3815777
hg1915777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3567949, esv3567950
Samples400683EC, 400075MR, 402063WM, 400207HN, 401899MB, 400177SJ
Known GenesDEFB123
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)dgv1241e212
Frequency
Sample Size873
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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