A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3571186



Internal ID18699384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55764219..55771483hg38UCSC Ensembl
Innerchr16:55798131..55805395hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387265
hg197265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv837e212
Supporting Variantsessv9811020, essv9811023, essv9811019, essv9811022
Samples401196CR, 400870KC, 401778CB, 401361GG
Known GenesCES1P1
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)esv3571186
Frequency
Sample Size873
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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