A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025289



Internal ID84587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78089951..78089951hg38UCSC Ensembl
chr9:80704867..80704867hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5399252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025289
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043656


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