A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17243403



Internal ID21690912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162424011..162424011hg38UCSC Ensembl
chr5:161851017..161851017hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5716417
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)nssv17243403
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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