A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198886



Internal ID20765926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45473007..45484519hg38UCSC Ensembl
chr19:45976265..45987777hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3811513
hg1911513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525893
Supporting Variants
Samples
Known GenesFOSB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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