A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237909



Internal ID21685418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128307401..128307401hg38UCSC Ensembl
chr5:127643093..127643093hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722437
Supporting Variants
Samples
Known GenesFBN2
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)nssv17237909
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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