A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5714457



Internal ID21740778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37768367..37768367hg38UCSC Ensembl
chr9:37768364..37768364hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17245762
Samples
Known GenesTRMT10B
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)nsv5714457
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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