A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093252



Internal ID21285174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:109046536..109076910hg38UCSC Ensembl
Innerchr11:108917263..108947637hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3830375
hg1930375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112596
Supporting Variants
Samplessample370
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093252
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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