A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091885



Internal ID21275759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5008289..5062577hg38UCSC Ensembl
Innerchr11:5029519..5083807hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854289
hg1954289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114229
Supporting Variants
Samplessample227
Known GenesOR52E2, OR52J3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091885
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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