A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702357



Internal ID21728678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92791306..92791306hg38UCSC Ensembl
chr10:94551063..94551063hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17189180
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)nsv5702357
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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