A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112889



Internal ID21296155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131908016..131914165hg38UCSC Ensembl
Innerchr11:131777910..131784059hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386150
hg196150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091855
Samplessample208
Known GenesNTM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112889
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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