A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1286e212



Internal ID20149742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19111102..19113482hg38UCSC Ensembl
chr22:19098615..19100995hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg382381
hg192381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3568251, esv3568250
Samples401067BD, 401104DM, 401478RD, 4000046CJ, 402061PI, 400681MC, 400371GA, 401602PR, 401977ES, 401281BP, 400482MD, 401311GL, 401180GR, 401079HJ, 400712GC, 402028BD, 400347VJ, 401100SJ, 400852WJ, 400704LC, 401695BT, 401251WN, 401730MS, 402008MC, 401623SN, 400620MT, 401437MJ, 401190WC, 400624RJ, 401119DK, 400268SY, 401025SM, 400158FB
Known GenesDGCR2
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)dgv1286e212
Frequency
Sample Size873
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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