A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5678163



Internal ID21704484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143561737..143561737hg38UCSC Ensembl
chr4:144482890..144482890hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17174691, nssv17209837
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)nsv5678163
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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