A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9821372



Internal ID18287850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23795497..24001082hg38UCSC Ensembl
Innerchr22:24137684..24353737hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38205586
hg19216054
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3575444
Supporting Variants
Samples400248JO
Known GenesDDT, DDTL, DERL3, GSTT2, GSTT2B, GSTTP1, LOC284889, MIF, SLC2A11, SMARCB1
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=252
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9821372
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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