A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116340



Internal ID21299606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27884331..28349674hg38UCSC Ensembl
Innerchr19:28375239..28840581hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38465344
hg19465343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101349
Samplessample300
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116340
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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