A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117252



Internal ID21300518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111344928..111349006hg38UCSC Ensembl
Innerchr11:111215653..111219731hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384079
hg194079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091950
Samplessample246
Known GenesMIR4491
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117252
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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