A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726633



Internal ID21752954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38919502..38919502hg38UCSC Ensembl
chr19:39410142..39410142hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17238433, nssv17252165
Samples
Known GenesSARS2
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5726633
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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