A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9794697



Internal ID18310739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96695997..96938929hg38UCSC Ensembl
Innerchr10:98455754..98698686hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38242933
hg19242933
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3577638
Supporting Variants
Samples400911GA
Known GenesLCOR, PIK3AP1
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
CommentsNumber of probes=192
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9794697
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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