A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9804659



Internal ID18310687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21951951..22501577hg38UCSC Ensembl
Innerchr14:22420174..22970561hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38549627
hg19550388
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3582960
Supporting Variants
Samples400911GA
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=794
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9804659
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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