A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522726



Internal ID298986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59780837..59811650hg38UCSC Ensembl
chr15:60073036..60103849hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3830814
hg1930814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522726
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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