A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242829



Internal ID22375393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91963831..91971549hg38UCSC Ensembl
Outerchr15:92507061..92514779hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258888
SamplesNA19238
Known GenesSLCO3A1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242829
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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