A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237059



Internal ID21684568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32937169..32937169hg38UCSC Ensembl
chr18:30517133..30517133hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728529
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)nssv17237059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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