A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696746



Internal ID21723067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130528472..130528472hg38UCSC Ensembl
chr10:132326736..132326736hg19UCSC Ensembl
Cytoband10q26.3
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 Variantsnssv17189438
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)nsv5696746
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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