A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17200794



Internal ID21648303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9605652..9605652hg38UCSC Ensembl
chr18:9605650..9605650hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5698750
Supporting Variants
Samples
Known GenesPPP4R1
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)nssv17200794
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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