A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17216035



Internal ID21663544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32637834..32637834hg38UCSC Ensembl
chr9:32637832..32637832hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5698488
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)nssv17216035
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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