A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093074



Internal ID21280297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26076327..26083076hg38UCSC Ensembl
Innerchr11:26097874..26104623hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg386750
hg196750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114831
Supporting Variants
Samplessample296
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093074
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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