A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17242718



Internal ID21690227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186607520..186607520hg38UCSC Ensembl
chr3:186325309..186325309hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381698
hg191698
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5720968
Supporting Variants
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)nssv17242718
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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