A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236325



Internal ID22373546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:17114447..17123974hg38UCSC Ensembl
Outerchr19:17225257..17234784hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14264029
SamplesNA19239
Known GenesMYO9B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236325
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