A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3572344



Internal ID18700542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155439592..155441357hg38UCSC Ensembl
Innerchr7:155232287..155234052hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9786374, essv9786391, essv9786387, essv9786381, essv9786397, essv9786383, essv9786384, essv9786386, essv9786389, essv9786401, essv9786375, essv9786379, essv9786398, essv9786393, essv9786382, essv9786400, essv9786402, essv9786392, essv9786396, essv9786373, essv9786394, essv9786395, essv9786385, essv9786376, essv9786390, essv9786403, essv9786378, essv9786380
Samples400906BR, 400429YF, 400655WB, 401824MM, 400298ME, 401297KC, 402029KJ, 400502GS, 401717LP, 400496BL, 400829MR, 400800MW, 400854SG, 400371GA, 400362TV, 401535RJ, 400722OM, 401844ZD, 400376SJ, 401012TP, 401054VM, 401314MK, 400769SL, 401543DC, 401681MS, 402042BJ, 401053MF, 401490TL
Known Genes
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)esv3572344
Frequency
Sample Size873
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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