A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583469



Internal ID18364981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50873350..50880505hg38UCSC Ensembl
Innerchr19:51376606..51383761hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387156
hg197156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1059e212
Supporting Variantsessv9817772, essv9817773
Samples401869BG, 401372RR
Known GenesKLK2
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)esv3583469
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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