A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3578621



Internal ID18706819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10898240..10906511hg38UCSC Ensembl
Innerchr10:10940203..10948474hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg388272
hg198272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv174e212
Supporting Variantsessv9792215, essv9792214, essv9792208, essv9792211, essv9792209, essv9792210, essv9792213
Samples401592NR, 400553PP, 400348DK, 402061PI, 401192MJ, 401251WN, 400601WC
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)esv3578621
Frequency
Sample Size873
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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