A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518298



Internal ID294693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46747304..46749764hg38UCSC Ensembl
chr15:47039502..47041962hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382461
hg192461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518298
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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