A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112489



Internal ID21295755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111386710..111389916hg38UCSC Ensembl
Innerchr11:111257435..111260641hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383207
hg193207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091159
Samplessample71
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112489
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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