A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090225



Internal ID21286372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68871407..68873564hg38UCSC Ensembl
Innerchr11:68638875..68641032hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg382158
hg192158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110622
Supporting Variants
Samplessample387
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090225
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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