A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226745



Internal ID20793785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25089401..25131100hg38UCSC Ensembl
chr8:24946916..24988615hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3841700
hg1941700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00039


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