A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226996



Internal ID22369618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:64968814..65032641hg38UCSC Ensembl
Outerchr13:65542946..65606773hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3863828
hg1963828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14256538
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226996
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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