A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3572135



Internal ID18700333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128959608..128969422hg38UCSC Ensembl
Innerchr7:128599662..128609476hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg389815
hg199815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9784979, essv9784962, essv9784973, essv9784976, essv9784975, essv9784980, essv9784974, essv9784958, essv9784959, essv9784965, essv9784953, essv9784957, essv9784967, essv9784972, essv9784964, essv9784961, essv9784956, essv9784970, essv9784969, essv9784963, essv9784954, essv9784960, essv9784971, essv9784968
Samples401749DJ, 400987FB, 400432VA, 400906BR, 401415CB, 400221VM, 401820SD, 400545EW, 400749VW, 401038LN, 400663MD, 401900RJ, 401027KW, 401477ST, 401804FG, 401813DN, 400050RL, 401952UH, 401414CR, 401884WJ, 401315HK, 402073LQ, 401817MC, 400525MR
Known GenesTNPO3
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)esv3572135
Frequency
Sample Size873
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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