A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17216441



Internal ID21663950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38475082..38475082hg38UCSC Ensembl
chr15:38767283..38767283hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714295
Supporting Variants
Samples
Known GenesFAM98B
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)nssv17216441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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