A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5730392



Internal ID21756713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131777128..131777128hg38UCSC Ensembl
chr8:132789375..132789375hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17235927
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)nsv5730392
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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