A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5720567



Internal ID21746888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173203011..173203011hg38UCSC Ensembl
chr1:173172150..173172150hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17237081
Samples
Known GenesTNFSF4
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)nsv5720567
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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