A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9775639



Internal ID18682693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98795801..98810855hg38UCSC Ensembl
Innerchr5:98131505..98146559hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3815055
hg1915055
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3570288
Supporting Variants
Samples401674DD
Known GenesRGMB
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
CommentsNumber of probes=16
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9775639
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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