A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115867



Internal ID21299133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121625087..121653379hg38UCSC Ensembl
Innerchr11:121495796..121524088hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3828293
hg1928293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090261
Samplessample398
Known GenesSORL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115867
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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