A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17252867



Internal ID21700376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63751944..63751944hg38UCSC Ensembl
chr16:63785848..63785848hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386010
hg196010
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5725316
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)nssv17252867
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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