A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112212



Internal ID21295478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10366403..10556962hg38UCSC Ensembl
Innerchr9:10366403..10556962hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38190560
hg19190560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088431
Samplessample19
Known GenesPTPRD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112212
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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