A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596655



Internal ID21788698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5476751..5477271hg38UCSC Ensembl
chr11:5497981..5498501hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032462
Supporting Variants
Samples
Known GenesOR51B5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596655
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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