A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044787



Internal ID97606
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 StatusS
Merged Variantsnsv5507080
Supporting Variants
Samples
Known GenesPRMT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044787
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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