A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17197882



Internal ID21645391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87629533..87629533hg38UCSC Ensembl
chr15:88172764..88172764hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5711616
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)nssv17197882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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