A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3580110



Internal ID18361622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10426165..10443276hg38UCSC Ensembl
Innerchr12:10578764..10595875hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3817112
hg1917112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv452e212
Supporting Variantsessv9800182, essv9800184, essv9800183, essv9800181
Samples401017SC, 401361GG, 401608GE, 401517PR
Known GenesKLRC2
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)esv3580110
Frequency
Sample Size873
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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