A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046615



Internal ID20613655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3701788..3711690hg38UCSC Ensembl
chr19:3701786..3711688hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389903
hg199903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533918
Supporting Variants
Samples
Known GenesTJP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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