A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17197712



Internal ID21645221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35952020..35952020hg38UCSC Ensembl
chr15:36244221..36244221hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5704118
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)nssv17197712
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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