A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112980



Internal ID21296246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11579712..11583148hg38UCSC Ensembl
Innerchr18:11579711..11583147hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv511n145
Supporting Variantsnssv14099556, nssv14099382, nssv14100176
Samplessample15, sample296, sample110
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112980
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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