A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041487



Internal ID95362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15786000..15795000hg38UCSC Ensembl
chr11:15807546..15816546hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041487
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002186


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