A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090261



Internal ID21287120
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 StatusS
Merged Variantsnsv3115867
Supporting Variants
Samplessample398
Known GenesSORL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090261
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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