A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9808188



Internal ID18324520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:239187428..239392293hg38UCSC Ensembl
Innerchr1:239350728..239555593hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38204866
hg19204866
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3575817
Supporting Variants
Samples401330RR
Known Genes
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
CommentsNumber of probes=130
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9808188
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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