A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5731057



Internal ID21757378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204212701..204212701hg38UCSC Ensembl
chr2:205077424..205077424hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252510, nssv17251456
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5731057
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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