A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3570844



Internal ID18352356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29869411..29906852hg38UCSC Ensembl
Innerchr6:29837188..29874629hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3837442
hg1937442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1726e212
Supporting Variantsessv9778484, essv9778486, essv9778482, essv9778495, essv9778483, essv9778488, essv9778498, essv9778487, essv9778481, essv9778485, essv9778494, essv9778497, essv9778490, essv9778496, essv9778493, essv9778492, essv9778491
Samples40031BA, 400906BR, 401582GG, 402064DC, 400203NA, 401791FG, 401192MJ, 400791GC, 401930GD, 400124FR, 401262RR, 401889FR, 401039PA, 400818BL, 401535RJ, 400712GC, 400072GR
Known GenesHLA-H
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)esv3570844
Frequency
Sample Size873
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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