A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3578121



Internal ID18359633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:115685413..115699886hg38UCSC Ensembl
Innerchr1:116228034..116242507hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3814474
hg1914474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv84e212
Supporting Variantsessv9786033, essv9786066, essv9785955, essv9786000, essv9786111, essv9786055, essv9786022, essv9785922, essv9786133, essv9785966, essv9785911, essv9785978, essv9786144, essv9786011, essv9786122, essv9786089, essv9785989, essv9785933, essv9786077, essv9785944, essv9786100, essv9786044
Samples401196CR, 400569WC, 400876OG, 401592NR, 400674CA, 401792KR, 400675HC, 401596PJ, 402056KD, 401977ES, 401981GF, 401875FG, 400371GA, 401011PJ, 400274TL, 400759FV, 402008MC, 401809FU, 402023EC, 401458RT, 400581VJ, 400532MH
Known GenesVANGL1
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)esv3578121
Frequency
Sample Size873
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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