A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718423



Internal ID21744744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16487331..16487331hg38UCSC Ensembl
chr19:16598142..16598142hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17250475
Samples
Known GenesCALR3
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)nsv5718423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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