A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091760



Internal ID21272163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125927661..125941225hg38UCSC Ensembl
Innerchr11:125797556..125811120hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813565
hg1913565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118180
Supporting Variants
Samplessample173
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091760
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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