A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240167



Internal ID22044777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114526800..114526800hg38UCSC Ensembl
chr9:117289080..117289080hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240167
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