A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578952



Internal ID21770995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86517373..86518090hg38UCSC Ensembl
chr9:89132288..89133005hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578952
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