A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244349



Internal ID22375835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:47853326..47959374hg38UCSC Ensembl
Outerchr19:48356583..48462631hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3874787
hg1974787
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4297n152
Supporting Variantsnssv14264771, nssv14264772, nssv14264773
SamplesNA19238, NA19239, HG00513
Known GenesSNAR-A1, SNAR-A10, SNAR-A11, SNAR-A12, SNAR-A13, SNAR-A14, SNAR-A2, SNAR-A3, SNAR-A4, SNAR-A5, SNAR-A6, SNAR-A7, SNAR-A8, SNAR-A9, SNAR-C1, SNAR-C2, SNAR-C3, SNAR-C4, SNAR-C5, SULT2A1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244349
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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