A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224773



Internal ID22368103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70037916..70038266hg38UCSC Ensembl
chr9:72652832..72653182hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346946, nssv14346949, nssv14346950, nssv14346947, nssv14346948, nssv14347566
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224773
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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