A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3575906



Internal ID18704104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177800537..177827951hg38UCSC Ensembl
Innerchr5:177227538..177254952hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3827415
hg1927415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1676e212
Supporting Variantsessv9776932, essv9776934, essv9776920, essv9776926, essv9776925, essv9776927, essv9776928, essv9776930, essv9776924, essv9776921, essv9776929, essv9776935, essv9776923, essv9776931
Samples400221VM, 401125LM, 401717LP, 401119DK, 400375KA, 401968HL, 400829MR, 401346FJ, 400598DA, 400444MM, 400722OM, 401628GC, 401882CR, 400269DA
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)esv3575906
Frequency
Sample Size873
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer