A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5677869



Internal ID21704190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14844257..14844257hg38UCSC Ensembl
chr3:14885764..14885764hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17208826
Samples
Known GenesFGD5
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)nsv5677869
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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