A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3570730



Internal ID18352242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2883674..2890049hg38UCSC Ensembl
Innerchr6:2883908..2890283hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg386376
hg196376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9777961, essv9777960
Samples400070PC, 401152MV
Known GenesSERPINB9
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)esv3570730
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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