A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726862



Internal ID21753183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77779635..77779635hg38UCSC Ensembl
chr5:77075459..77075459hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17241165
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)nsv5726862
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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