A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223381



Internal ID22367170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67784938..67795565hg38UCSC Ensembl
chr10:69544696..69555323hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810628
hg1910628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv971n152
Supporting Variantsnssv14351750, nssv14351749
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223381
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