A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839897



Internal ID22023540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22674302..22674302hg38UCSC Ensembl
chr8:22531815..22531815hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839897
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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