A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9815326



Internal ID18673055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80630279..80637924hg38UCSC Ensembl
Innerchr17:78604079..78611724hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg387646
hg197646
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3573853
Supporting Variants
Samples401377MA
Known GenesRPTOR
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=20
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9815326
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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