A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5716294



Internal ID21742615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48458780..48458780hg38UCSC Ensembl
chr16:48492691..48492691hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252669
Samples
Known Genes
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)nsv5716294
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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