A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14269349



Internal ID22136096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:16021340..16095759hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3874420
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228557
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14269349
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