A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17190441



Internal ID21637950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19057930..19057930hg38UCSC Ensembl
chr11:19079477..19079477hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5703547
Supporting Variants
Samples
Known GenesMRGPRX2
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)nssv17190441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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