A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258441



Internal ID22201114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:62403019..62421180hg38UCSC Ensembl
Outerchr15:62695218..62713379hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818162
hg1918162
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216920
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258441
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