A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5724435



Internal ID21750756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72106180..72106180hg38UCSC Ensembl
chr15:72398521..72398521hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17237530, nssv17252979
Samples
Known GenesMYO9A
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)nsv5724435
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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