A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3581605



Internal ID18363117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52294887..52388067hg38UCSC Ensembl
Innerchr12:52688671..52781851hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3893181
hg1993181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv487e212
Supporting Variantsessv9801387, essv9801385, essv9801386, essv9801384
Samples401766MR, 401091HS, 401284NA, 402024BB
Known GenesKRT83, KRT84, KRT85, KRT86
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)esv3581605
Frequency
Sample Size873
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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