A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236582



Internal ID21684091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38430545..38430545hg38UCSC Ensembl
chr13:39004682..39004682hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381815
hg191815
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5727119
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)nssv17236582
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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