A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3580490



Internal ID18362002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:117134116..117150922hg38UCSC Ensembl
Innerchr12:117571921..117588727hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg3816807
hg1916807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv520e212
Supporting Variantsessv9802497
Samples400344DR
Known GenesFBXO21
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)esv3580490
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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