A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840362



Internal ID22024005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102822684..102822684hg38UCSC Ensembl
chr8:103834912..103834912hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840362
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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