A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14275573



Internal ID22136097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:11354348..11370157hg38UCSC Ensembl
Outerchr10:11396347..11412156hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3815810
hg1915810
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210790
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14275573
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