A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17249561



Internal ID21697070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98319511..98319511hg38UCSC Ensembl
chr6:98767387..98767387hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5730629
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)nssv17249561
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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