A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3578478



Internal ID18706676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233288306..233292603hg38UCSC Ensembl
Innerchr1:233424052..233428349hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg384298
hg194298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9807266, essv9807311, essv9807211, essv9807244, essv9807288, essv9807188, essv9807333, essv9807255, essv9807277, essv9807200, essv9807299, essv9807177, essv9807322, essv9807222, essv9807355, essv9807233, essv9807344
Samples400287BP, 401380OL, 401195PN, 400948EV, 400307HW, 401050GS, 400383HL, 401027KW, 400240HJ, 401526WB, 401419SW, 400014SL, 401112LG, 401010HT, 402008MC, 400079AP, 400890IT
Known GenesPCNXL2
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)esv3578478
Frequency
Sample Size873
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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