A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3576607



Internal ID18704805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129779957..129839982hg38UCSC Ensembl
Innerchr8:130792203..130852228hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3860026
hg1960026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9789899
Samples401986LC
Known GenesFAM49B, GSDMC
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)esv3576607
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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