A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190581



Internal ID22341426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1519170..1549845hg38UCSC Ensembl
Outerchr4:1520897..1551572hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3830676
hg1930676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6384n152
Supporting Variantsnssv14272287
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190581
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