A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842409



Internal ID22026052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92472379..92472379hg38UCSC Ensembl
chr10:94232136..94232136hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247377
Supporting Variants
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842409
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