A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3580496



Internal ID18708694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:117877067..117879275hg38UCSC Ensembl
Innerchr12:118314872..118317080hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg382209
hg192209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9802521, essv9802520, essv9802523
Samples400802DP, 402051AF, 401314MK
Known GenesKSR2
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)esv3580496
Frequency
Sample Size873
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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