A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212624



Internal ID22359810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37552581..37553200hg38UCSC Ensembl
chr9:37552578..37553197hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346509
SamplesNA19239
Known GenesFBXO10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212624
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