A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845096



Internal ID22028739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80140468..80140468hg38UCSC Ensembl
chr13:80714603..80714603hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845096
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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