A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5725017



Internal ID21751338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77269909..77269909hg38UCSC Ensembl
chr3:77319060..77319060hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17236411
Samples
Known GenesROBO2
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)nsv5725017
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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