A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617095



Internal ID21809142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89376225..89376283hg38UCSC Ensembl
chr15:89919456..89919514hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617095
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