A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3581376



Internal ID18709574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:88223148..88233049hg38UCSC Ensembl
Innerchr14:88689492..88699393hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg389902
hg199902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9807113
Samples400526DR
Known GenesKCNK10
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)esv3581376
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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