A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463389



Internal ID241293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95631226..95631341hg38UCSC Ensembl
chr5:94966930..94967045hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463389
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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