A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5694666



Internal ID21720987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109960761..109960761hg38UCSC Ensembl
chr10:111720519..111720519hg19UCSC Ensembl
Cytoband10q25.1
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 Variantsnssv17189750, nssv17230557
Samples
Known GenesADD3-AS1
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)nsv5694666
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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