A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226694



Internal ID22369408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:130217359..130229504hg38UCSC Ensembl
Outerchr10:132015623..132027768hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3812146
hg1912146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112n152
Supporting Variantsnssv14279248, nssv14279249
SamplesNA19240, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226694
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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