A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3570483



Internal ID18351995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147010968..147017790hg38UCSC Ensembl
Innerchr5:146390531..146397353hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386823
hg196823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1656e212
Supporting Variantsessv9776350, essv9776349
Samples401477ST, 401952UH
Known GenesPPP2R2B
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)esv3570483
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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