A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17234870



Internal ID21682379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30999357..30999357hg38UCSC Ensembl
chr18:28579323..28579323hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5717434
Supporting Variants
Samples
Known GenesDSC3
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)nssv17234870
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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