A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709061



Internal ID21735382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81582179..81582179hg38UCSC Ensembl
chr14:82048523..82048523hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17214354
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)nsv5709061
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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