A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702160



Internal ID21728481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97450586..97450586hg38UCSC Ensembl
chr9:100212868..100212868hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17186744
Samples
Known GenesTDRD7
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)nsv5702160
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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