A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093192



Internal ID21283468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91073866..91119912hg38UCSC Ensembl
Innerchr11:90807034..90853080hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3846047
hg1946047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117511
Supporting Variants
Samplessample345
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093192
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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