A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3576312



Internal ID18357824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38255382..38338531hg38UCSC Ensembl
Innerchr7:38294983..38378132hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3883150
hg1983150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1888e212
Supporting Variantsessv9783377, essv9783376
Samples400294HD, 400588BE
Known GenesTARP
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)esv3576312
Frequency
Sample Size873
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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