A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17249853



Internal ID21697362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99517120..99517120hg38UCSC Ensembl
chr13:100169374..100169374hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728075
Supporting Variants
Samples
Known GenesTM9SF2
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)nssv17249853
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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