A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17228432



Internal ID21675941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189859295..189859295hg38UCSC Ensembl
chr2:190724021..190724021hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5682997
Supporting Variants
Samples
Known GenesPMS1
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)nssv17228432
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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