A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3570457



Internal ID18351969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140839141..140863322hg38UCSC Ensembl
Innerchr5:140218726..140242907hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3824182
hg1924182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1652e212
Supporting Variantsessv9776295, essv9776306, essv9776302, essv9776307, essv9776309, essv9776298, essv9776313, essv9776301, essv9776297, essv9776305, essv9776314, essv9776300, essv9776308, essv9776303, essv9776312, essv9776294, essv9776304, essv9776296
Samples400599CP, 401962BK, 401733CG, 400059SV, 400688FL, 400148MS, 400007RG, 401513KC, 401346FJ, 400047DS, 401919MD, 401940SJ, 400728PB, 400156WT, 400859SC, 401458RT, 400213DB, 400238BB
Known GenesPCDHA1, PCDHA10, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
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)esv3570457
Frequency
Sample Size873
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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