A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278741



Internal ID20487959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117843401..117843401hg38UCSC Ensembl
chr9:120605679..120605679hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278741
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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