A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3576027



Internal ID18704225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17268315..17292802hg38UCSC Ensembl
Innerchr1:17594810..17619297hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3824488
hg1924488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv19e212
Supporting Variantsessv9801533
Samples401825TH
Known GenesPADI3
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)esv3576027
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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