A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17251386



Internal ID21698895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80321500..80321500hg38UCSC Ensembl
chr4:81242654..81242654hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5720164
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)nssv17251386
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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