A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9780707



Internal ID18678653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78135248..78157419hg38UCSC Ensembl
Innerchr6:78844965..78867136hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3822172
hg1922172
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3571238
Supporting Variants
Samples401535RJ
Known Genes
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)essv9780707
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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