A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725633



Internal ID21751954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64720558..64720558hg38UCSC Ensembl
chr2:64947692..64947692hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17245552
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)nsv5725633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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