A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5677222



Internal ID21703543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14358410..14358410hg38UCSC Ensembl
chr6:14358641..14358641hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17179187
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)nsv5677222
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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