A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3580683



Internal ID18708881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58507860..58519120hg38UCSC Ensembl
Innerchr13:59081994..59093254hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3811261
hg1911261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9803509, essv9803512, essv9803510
Samples400453LN, 400155CW, 401652HL
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
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3580683
Frequency
Sample Size873
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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