A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3571594



Internal ID18699792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6797362..6814451hg38UCSC Ensembl
Innerchr7:6836993..6854082hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3817090
hg1917090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1867e212
Supporting Variantsessv9782912, essv9782914, essv9782920, essv9782919, essv9782918, essv9782917, essv9782910, essv9782923, essv9782921, essv9782924, essv9782913, essv9782915, essv9782916
Samples400340CD, 400493KH, 400579HJ, 400040CN, 400543CK, 401011PJ, 401112LG, 401514BA, 401881TJ, 400759FV, 400778SR, 400835FD, 400138LA
Known GenesCCZ1B, RSPH10B, RSPH10B2
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)esv3571594
Frequency
Sample Size873
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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