A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226091



Internal ID22369017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134135131..134137027hg38UCSC Ensembl
chr9:137000253..137002149hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381897
hg191897
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347873, nssv14347874, nssv14347878, nssv14347870, nssv14347876, nssv14347872, nssv14347877, nssv14347871, nssv14347875
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesWDR5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226091
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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