A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099352



Internal ID21272058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:21650080..21725529hg38UCSC Ensembl
Innerchr18:19230041..19305490hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3875450
hg1975450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115313
Supporting Variants
Samplessample171
Known GenesABHD3, MIR320C1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099352
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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