A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723292



Internal ID146958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38919502..38919553hg38UCSC Ensembl
chr19:39410142..39410193hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561343
Supporting Variants
Samples
Known GenesSARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723292
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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