A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237085



Internal ID21684594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55291603..55291603hg38UCSC Ensembl
chr12:55685387..55685387hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726726
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)nssv17237085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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