A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17210329



Internal ID21657838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25777976..25777976hg38UCSC Ensembl
chr3:25819467..25819467hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5677496
Supporting Variants
Samples
Known GenesNGLY1
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)nssv17210329
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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