A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5676928



Internal ID21703249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51328360..51328360hg38UCSC Ensembl
chr1:51794032..51794032hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17221465, nssv17205143
Samples
Known GenesTTC39A
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)nsv5676928
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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