A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516161



Internal ID292627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41338281..41338680hg38UCSC Ensembl
chr19:41844186..41844585hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723488
Samples
Known GenesTGFB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516161
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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