A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839655



Internal ID22023298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59129793..59129793hg38UCSC Ensembl
chr8:60042352..60042352hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839655
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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