A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583653



Internal ID18711851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15578113..15590486hg38UCSC Ensembl
Innerchr2:15718237..15730610hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3812374
hg1912374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9815177, essv9815166, essv9815288, essv9815133, essv9815188, essv9815033, essv9815255, essv9815155, essv9815322, essv9815299, essv9815122, essv9815044, essv9815144, essv9815211, essv9815333, essv9815200, essv9815233, essv9815089, essv9815244, essv9815311, essv9815066, essv9815266, essv9815077, essv9815100, essv9815222, essv9815344, essv9815277, essv9815055, essv9815355, essv9815111
Samples401400NP, 400336BG, 401956DQ, 400140WM, 401468RL, 401551MB, 400298ME, 401239PR, 400148MS, 400231LP, 400460DM, 401029SD, 401234MB, 400041LJ, 401448BJ, 401499JR, 401091HS, 401913GT, 400207HN, 401318AV, 401859GS, 401580CA, 400135DR, 400611GG, 401182OC, 400654YW, 400542EG, 400845ML, 400410CD, 401763SG
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)esv3583653
Frequency
Sample Size873
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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