A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839925



Internal ID22023568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79594581..79594581hg38UCSC Ensembl
chr8:80506816..80506816hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246200
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839925
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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