A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17213487



Internal ID21660996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63865403..63865403hg38UCSC Ensembl
chr6:64575296..64575296hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5687170
Supporting Variants
Samples
Known GenesEYS
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)nssv17213487
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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