A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3581265



Internal ID18709463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69546071..69565993hg38UCSC Ensembl
Innerchr14:70012788..70032710hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3819923
hg1919923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv650e212
Supporting Variantsessv9806343, essv9806334, essv9806331, essv9806330, essv9806338, essv9806339, essv9806342, essv9806335, essv9806341, essv9806340, essv9806336, essv9806332, essv9806337
Samples401673DM, 400230TB, 401384BP, 400528LR, 401326LI, 400888MS, 401875FG, 400135DR, 401428LD, 401881TJ, 400769SL, 400323AA, 400238BB
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
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3581265
Frequency
Sample Size873
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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