A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5687122



Internal ID21713443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26605344..26605344hg38UCSC Ensembl
chr6:26605572..26605572hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17177281, nssv17222045
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)nsv5687122
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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