A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5689026



Internal ID21715347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:70505611..70505611hg38UCSC Ensembl
chr7:69970597..69970597hg19UCSC Ensembl
Cytoband7q11.22
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 Variantsnssv17181969
Samples
Known GenesAUTS2
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)nsv5689026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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