A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9805949



Internal ID18334905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66586328..66656920hg38UCSC Ensembl
Innerchr14:67053046..67123638hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3870593
hg1970593
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3581240
Supporting Variants
Samples401623SN
Known GenesGPHN
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=103
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9805949
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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