A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv594e212



Internal ID20149050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21951951..22526820hg38UCSC Ensembl
chr14:22420174..22995788hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38574870
hg19575615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3583004, esv3583115, esv3583049, esv3583104, esv3583027, esv3583082, esv3582960, esv3583071, esv3582927, esv3583093, esv3583015, esv3582982, esv3582971, esv3583138, esv3583126, esv3583038, esv3582993, esv3583060
Samples400911GA, 401734PG, 400622SJ, 400528LR, 401990PR, 400588BE, 400320RN, 400374LB, 400113LD, 401448BJ, 401262RR, 400450FG, 401410BJ, 401354KM, 400508RD, 401612HB, 401576WC, 401510DG, 401068SD
Known Genes
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)dgv594e212
Frequency
Sample Size873
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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