A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9817266



Internal ID18347529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32408603..33109240hg38UCSC Ensembl
Innerchr2:32633671..33334307hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38700638
hg19700637
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3575217
Supporting Variants
Samples402009WP
Known GenesBIRC6, LINC00486, LOC100271832, LTBP1, MIR4765, MIR558, TTC27
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=766
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9817266
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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