A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5689083



Internal ID21715404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54855934..54855934hg38UCSC Ensembl
chr1:55321607..55321607hg19UCSC Ensembl
Cytoband1p32.3
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 Variantsnssv17218975
Samples
Known GenesDHCR24
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)nsv5689083
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer