A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5710662



Internal ID21736983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93670882..93670882hg38UCSC Ensembl
chr10:95430639..95430639hg19UCSC Ensembl
Cytoband10q23.33
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 Variantsnssv17188869
Samples
Known GenesFRA10AC1
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)nsv5710662
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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