A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593899



Internal ID21785942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21319677..21319677hg38UCSC Ensembl
chr9:21319676..21319676hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593899
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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