A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9775105



Internal ID18688804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:60190687..60208327hg38UCSC Ensembl
Innerchr5:59486514..59504154hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3817641
hg1917641
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3570167
Supporting Variants
Samples401855RE
Known GenesPDE4D
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
CommentsNumber of probes=10
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9775105
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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