A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726152



Internal ID21752473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25859911..25859911hg38UCSC Ensembl
chr2:26082780..26082780hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17239974
Samples
Known GenesASXL2
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)nsv5726152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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