A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841487



Internal ID22025130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77669816..77669816hg38UCSC Ensembl
chr9:80284732..80284732hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841487
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