A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227367



Internal ID20794407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141266201..141313816hg38UCSC Ensembl
chr8:142276300..142323915hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3847616
hg1947616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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