A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046254



Internal ID98639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67562615..67564980hg38UCSC Ensembl
chr11:67330086..67332451hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046254
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008586


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