A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840546



Internal ID22024189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25634801..25634801hg38UCSC Ensembl
chr8:25492317..25492317hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840546
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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