A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3568492



Internal ID18350004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:49924599..49933235hg38UCSC Ensembl
Innerchr22:50318247..50326883hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg388637
hg198637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1335e212
Supporting Variantsessv9822593, essv9822594
Samples401801LA, 400849SH
Known GenesCRELD2
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)esv3568492
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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