A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540887



Internal ID315578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24510073..24510073hg38UCSC Ensembl
chr16:24521394..24521394hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540887
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer