A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5724515



Internal ID21750836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89922250..89922250hg38UCSC Ensembl
chr15:90465482..90465482hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381305
hg191305
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17241886, nssv17242868
Samples
Known Genes
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)nsv5724515
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer