A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17180110



Internal ID21627619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108022934..108022934hg38UCSC Ensembl
chr6:108344138..108344138hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5687680
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)nssv17180110
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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