A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14273521



Internal ID22232092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38726208..38761018hg38UCSC Ensembl
Outerchr4:38727829..38762639hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381568
hg191568
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225616
Supporting Variants
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14273521
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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