A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583673



Internal ID18365185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25797581..25819474hg38UCSC Ensembl
Innerchr2:26020450..26042343hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3821894
hg1921894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1103e212
Supporting Variantsessv9816388
Samples401054VM
Known GenesASXL2
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)esv3583673
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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