A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5680445



Internal ID21706766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148826215..148826215hg38UCSC Ensembl
chr3:148544002..148544002hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17226281
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5680445
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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