A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240087



Internal ID22044697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105175186..105175186hg38UCSC Ensembl
chr9:107937467..107937467hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240087
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