A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110521



Internal ID21293787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125214461..125239607hg38UCSC Ensembl
Innerchr11:125084357..125109503hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3825147
hg1925147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091759
Samplessample172
Known GenesPKNOX2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110521
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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