A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3575209



Internal ID18356721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:27334578..27389381hg38UCSC Ensembl
Innerchr2:27557445..27612248hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3854804
hg1954804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9816466
Samples400337HG
Known GenesEIF2B4, GTF3C2, LOC100505624, PPM1G, SNX17, ZNF513
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)esv3575209
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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