A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115098



Internal ID21298364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127752770..127785428hg38UCSC Ensembl
Innerchr11:127622665..127655323hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3832659
hg1932659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091088
Samplessample46
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115098
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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