A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17221836



Internal ID21669345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51891723..51891723hg38UCSC Ensembl
chr15:52183920..52183920hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5712015
Supporting Variants
Samples
Known GenesTMOD3
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)nssv17221836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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