A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237296



Internal ID21684805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27966429..27966429hg38UCSC Ensembl
chr11:27987976..27987976hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722433
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)nssv17237296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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