A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195984



Internal ID22346078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:35225633..35294786hg38UCSC Ensembl
Outerchr4:35227255..35296408hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3869154
hg1969154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6549n152
Supporting Variantsnssv14272832
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195984
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