A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229009



Internal ID22370998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:106851330..106866795hg38UCSC Ensembl
Outerchr13:107503678..107519143hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3815466
hg1915466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14256550
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229009
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