A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583864



Internal ID18365376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:73250085..73260879hg38UCSC Ensembl
Innerchr2:73477213..73488007hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3810795
hg1910795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9827621, essv9827610
Samples401297KC, 401234MB
Known GenesCCT7, FBXO41
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)esv3583864
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer