A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047106



Internal ID20614146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48942930..48945190hg38UCSC Ensembl
chr19:49446187..49448447hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382261
hg192261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532498
Supporting Variants
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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