A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3578824



Internal ID18360336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46402446..46572146hg38UCSC Ensembl
Innerchr10:46977471..47147301hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38169701
hg19169831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218e212
Supporting Variantsessv9793304
Samples402074RR
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
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)esv3578824
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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