A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098994



Internal ID21288146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30221739..30230771hg38UCSC Ensembl
Innerchr19:30712646..30721678hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg389033
hg199033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111582
Supporting Variants
Samplessample412
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098994
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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