A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115858



Internal ID21299124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94026867..94052818hg38UCSC Ensembl
Innerchr9:96789149..96815100hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3825952
hg1925952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087994
Samplessample283
Known GenesPTPDC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115858
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