A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9810582



Internal ID18688957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32542905..34007842hg38UCSC Ensembl
Innerchr16:32554226..33810309hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381464938
hg191256084
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3570698
Supporting Variants
Samples401856GC
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
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=175
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9810582
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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