A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17233681



Internal ID21681190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58103002..58103002hg38UCSC Ensembl
chr8:59015561..59015561hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5727933
Supporting Variants
Samples
Known GenesFAM110B
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)nssv17233681
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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