A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111036



Internal ID21294302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37021606..37029516hg38UCSC Ensembl
Innerchr11:37043156..37051066hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387911
hg197911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093049
Samplessample289
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111036
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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