A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5707817



Internal ID21734138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105006017..105006017hg38UCSC Ensembl
chr13:105658368..105658368hg19UCSC Ensembl
Cytoband13q33.2
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 Variantsnssv17195359
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)nsv5707817
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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