A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093199



Internal ID21283652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65856159..65859723hg38UCSC Ensembl
Innerchr11:65623630..65627194hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383565
hg193565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114832
Supporting Variants
Samplessample348
Known GenesCFL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093199
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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