A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198992



Internal ID20766032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6533599..6577552hg38UCSC Ensembl
chr19:6533610..6577563hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3843954
hg1943954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518918
Supporting Variants
Samples
Known GenesTNFSF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198992
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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