A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17197820



Internal ID21645329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70782736..70782736hg38UCSC Ensembl
chr15:71075075..71075075hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5711123
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)nssv17197820
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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