A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3568348



Internal ID18349860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27986182..28002208hg38UCSC Ensembl
Innerchr22:28382170..28398196hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3816027
hg1916027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9821990
Samples401258PC
Known GenesTTC28, TTC28-AS1
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)esv3568348
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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