A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088811



Internal ID21286197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85383278..85386992hg38UCSC Ensembl
Innerchr9:87998193..88001907hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383715
hg193715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115368
Supporting Variants
Samplessample385
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088811
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