A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3576492



Internal ID18704690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155671323..155682822hg38UCSC Ensembl
Innerchr7:155464017..155475516hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811500
hg1911500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9786407, essv9786428, essv9786427, essv9786425, essv9786412, essv9786408, essv9786429, essv9786419, essv9786426, essv9786423, essv9786417, essv9786420, essv9786406, essv9786411, essv9786416, essv9786415, essv9786414, essv9786418, essv9786424, essv9786413, essv9786405, essv9786409
Samples401474CE, 400287BP, 400987FB, 400619MP, 401742KB, 400083TG, 401927SK, 401931JL, 401582GG, 400526DR, 400582WS, 400070PC, 401863BD, 401862AN, 400547BS, 400444MM, 401858TP, 400205SP, 402073LQ, 400084DM, 401395OP, 400234CA
Known GenesRBM33
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)esv3576492
Frequency
Sample Size873
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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