A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185721



Internal ID20752761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67027701..67029900hg38UCSC Ensembl
chr16:67061604..67063803hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500172
Supporting Variants
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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