A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5723372



Internal ID21749693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70393794..70393794hg38UCSC Ensembl
chr15:70686133..70686133hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17251251
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)nsv5723372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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