A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725773



Internal ID21752094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88472606..88472606hg38UCSC Ensembl
chr8:89484835..89484835hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17233584
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)nsv5725773
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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