A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091950



Internal ID21277176
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 StatusS
Merged Variantsnsv3117252
Supporting Variants
Samplessample246
Known GenesMIR4491
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091950
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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