A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594278



Internal ID21786321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96083227..96083227hg38UCSC Ensembl
chr9:98845509..98845509hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091074
Supporting Variants
Samples
Known GenesLOC158435
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594278
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