A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5716052



Internal ID21742373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48892962..48892962hg38UCSC Ensembl
chr12:49286745..49286745hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17244402
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)nsv5716052
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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