A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17185343



Internal ID21632852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72058496..72058496hg38UCSC Ensembl
chr8:72970731..72970731hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5707620
Supporting Variants
Samples
Known GenesTRPA1
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)nssv17185343
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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