A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9790220



Internal ID18688981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6902404..7245728hg38UCSC Ensembl
Innerchr9:6902404..7245728hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38343325
hg19343325
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3576622
Supporting Variants
Samples401856GC
Known GenesKDM4C
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=516
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9790220
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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