A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846450



Internal ID22030093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45384149..45384149hg38UCSC Ensembl
chr15:45676347..45676347hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846450
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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