A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5714896



Internal ID21741217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4149200..4149200hg38UCSC Ensembl
chr5:4149313..4149313hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17238599
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)nsv5714896
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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