A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17185353



Internal ID21632862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72515516..72515516hg38UCSC Ensembl
chr8:73427751..73427751hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714085
Supporting Variants
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)nssv17185353
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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