A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115256



Internal ID21298522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48305041..48308089hg38UCSC Ensembl
Innerchr10:49513084..49516132hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383049
hg193049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088953
Samplessample24
Known GenesMAPK8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115256
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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