A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17244797



Internal ID21692306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124546681..124546681hg38UCSC Ensembl
chr5:123882374..123882374hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg384077
hg194077
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726812
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)nssv17244797
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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