A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726833



Internal ID21753154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140957081..140957081hg38UCSC Ensembl
chr3:140675923..140675923hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17243599
Samples
Known GenesSLC25A36
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5726833
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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