A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113249



Internal ID21296515
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 StatusM
Merged Variants
Supporting Variantsnssv14099374
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113249
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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