A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17178689



Internal ID21626198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18496392..18496392hg38UCSC Ensembl
chr6:18496623..18496623hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5685875
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)nssv17178689
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer