A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194021



Internal ID20761061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82463486..82479484hg38UCSC Ensembl
chr16:82497091..82513089hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3815999
hg1915999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513242
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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