A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025522



Internal ID84746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99670518..99670569hg38UCSC Ensembl
chr9:102432800..102432851hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5411437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025522
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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