A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682665



Internal ID21708986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25045737..25045737hg38UCSC Ensembl
chr6:25045965..25045965hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17179491, nssv17216124
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)nsv5682665
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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