A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198123



Internal ID20765163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3943849..3952784hg38UCSC Ensembl
chr19:3943847..3952782hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388936
hg198936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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