A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17217668



Internal ID21665177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163366208..163366208hg38UCSC Ensembl
chr6:163787240..163787240hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5680021
Supporting Variants
Samples
Known Genes
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)nssv17217668
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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