A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236013



Internal ID21683522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101369393..101369393hg38UCSC Ensembl
chr3:101088237..101088237hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5715412
Supporting Variants
Samples
Known GenesSENP7
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)nssv17236013
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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