A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195900



Internal ID22346003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:146251699..146260577hg38UCSC Ensembl
Outerchr3:145969486..145978364hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg388879
hg198879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271720
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195900
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