A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259868



Internal ID22064478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158967746..158967746hg38UCSC Ensembl
chr3:158685535..158685535hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259868
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