A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3575371



Internal ID18356883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36629297..36654563hg38UCSC Ensembl
Innerchr20:35257700..35282966hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3825267
hg1925267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9819432
Samples401687LR
Known GenesNDRG3, SLA2
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)esv3575371
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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