A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679923



Internal ID21706244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66983026..66983026hg38UCSC Ensembl
chr2:67210158..67210158hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17205118
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)nsv5679923
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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