A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726595



Internal ID21752916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70420011..70420011hg38UCSC Ensembl
chr1:70885694..70885694hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17241448
Samples
Known GenesCTH
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)nsv5726595
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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