A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577900



Internal ID18359412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:62299377..62306529hg38UCSC Ensembl
Innerchr1:62765049..62772200hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387153
hg197152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9768090, essv9768078, essv9768056, essv9768067, essv9768034, essv9768045
Samples400649PS, 401869BG, 401311GL, 400869BK, 401039PA, 401413RG
Known GenesKANK4
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)esv3577900
Frequency
Sample Size873
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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