A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842420



Internal ID22026063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94329444..94329444hg38UCSC Ensembl
chr10:96089201..96089201hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842420
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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