A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17240192



Internal ID21687701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107601131..107601131hg38UCSC Ensembl
chr10:109360889..109360889hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5727736
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)nssv17240192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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