A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17250362



Internal ID21697871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206995977..206995977hg38UCSC Ensembl
chr2:207860701..207860701hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382828
hg192828
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5729522
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)nssv17250362
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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