A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3582888



Internal ID18364400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68079784..68102188hg38UCSC Ensembl
Innerchr17:66075889..66098329hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3822405
hg1922441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9815261
Samples400128MJ
Known GenesLINC00674
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)esv3582888
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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