A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567999



Internal ID18349511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47286294..47301900hg38UCSC Ensembl
Innerchr20:45915038..45930644hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3815607
hg1915607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9819709, essv9819711, essv9819708, essv9819707
Samples400582WS, 400763BT, 401861GG, 401143LK
Known GenesZMYND8
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)esv3567999
Frequency
Sample Size873
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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