A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17242934



Internal ID21690443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110919496..110919496hg38UCSC Ensembl
chr11:110790220..110790220hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5716012
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)nssv17242934
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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