A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099416



Internal ID21282636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30745398..30843963hg38UCSC Ensembl
Innerchr18:28325364..28423929hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3898566
hg1998566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116463
Supporting Variants
Samplessample33
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099416
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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