A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5708876



Internal ID21735197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35790070..35790070hg38UCSC Ensembl
chr9:35790067..35790067hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17186147
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)nsv5708876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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