A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045219



Internal ID97896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65436492..65443577hg38UCSC Ensembl
chr11:65203963..65211048hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387086
hg197086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045219
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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