A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3581255



Internal ID18362767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67186338..67191396hg38UCSC Ensembl
Innerchr14:67653055..67658113hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9805982, essv9805986, essv9805985, essv9805983, essv9805984
Samples401077VC, 400486LS, 401725MR, 401940SJ, 401361GG
Known GenesFAM71D
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)esv3581255
Frequency
Sample Size873
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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