A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841521



Internal ID22025164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116477861..116477861hg38UCSC Ensembl
chr9:119240140..119240140hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240181
Supporting Variants
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841521
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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