A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3575984



Internal ID18704182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:294911..381137hg38UCSC Ensembl
Innerchr6:294911..381137hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3886227
hg1986227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1705e212
Supporting Variantsessv9777911, essv9777918, essv9777919, essv9777916, essv9777908, essv9777915, essv9777904, essv9777909, essv9777905, essv9777903, essv9777902, essv9777910, essv9777917, essv9777906, essv9777900, essv9777914, essv9777907, essv9777913
Samples400911GA, 401146US, 401824MM, 400033KC, 401550SP, 400442FE, 401027KW, 402033WD, 401477ST, 401526WB, 400171BJ, 401359HF, 400728PB, 400792RE, 401543DC, 401607LL, 401882CR, 400138LA
Known GenesDUSP22
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)esv3575984
Frequency
Sample Size873
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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