A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3568377



Internal ID18349889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33777442..33785393hg38UCSC Ensembl
Innerchr22:34173429..34181380hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg387952
hg197952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1314e212
Supporting Variantsessv9822097, essv9822093, essv9822085, essv9822096, essv9822089, essv9822084, essv9822090, essv9822094, essv9822092, essv9822091, essv9822098, essv9822086, essv9822095
Samples401235IA, 400906BR, 401911FL, 400834SS, 401173AI, 401281BP, 400002HK, 401563TK, 400265LK, 401619BT, 400249BC, 401086MD, 400540BM
Known GenesLARGE
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)esv3568377
Frequency
Sample Size873
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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