A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209340



Internal ID22357435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:34618593..34655429hg38UCSC Ensembl
Outerchr1:35084194..35121030hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3836837
hg1936837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14256594, nssv14256593
SamplesHG00731, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209340
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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