A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5726569



Internal ID21752890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31145601..31145601hg38UCSC Ensembl
chr15:31437804..31437804hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17251105
Samples
Known GenesTRPM1
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)nsv5726569
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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