A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17251054



Internal ID21698563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118263060..118263060hg38UCSC Ensembl
chr1:118805683..118805683hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721385
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)nssv17251054
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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