A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559813



Internal ID21884168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117687039..117687160hg38UCSC Ensembl
chr6:118008202..118008323hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014259
Supporting Variants
Samples
Known GenesNUS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559813
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