A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5701738



Internal ID21728059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36055786..36055786hg38UCSC Ensembl
chr21:37428084..37428084hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17204386
Samples
Known GenesSETD4
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)nsv5701738
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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