A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507080



Internal ID283809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20443736..20444096hg38UCSC Ensembl
chr11:20465282..20465642hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044787
Samples
Known GenesPRMT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507080
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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