A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9794885



Internal ID18327263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113598193..113692546hg38UCSC Ensembl
Innerchr10:115357952..115452305hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3894354
hg1994354
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3577738
Supporting Variants
Samples401402EN
Known GenesCASP7, NRAP
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=112
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9794885
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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