A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099374



Internal ID21272792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35717196..35732833hg38UCSC Ensembl
Innerchr18:33297160..33312797hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3815638
hg1915638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113249
Supporting Variants
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099374
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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