A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5714849



Internal ID21741170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43086386..43086386hg38UCSC Ensembl
chr15:43378584..43378584hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17247628
Samples
Known GenesUBR1
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)nsv5714849
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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