A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041525



Internal ID95383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17062683..17065581hg38UCSC Ensembl
chr11:17084230..17087128hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382899
hg192899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041525
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004683


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