A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089750



Internal ID21271058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122293225..122304765hg38UCSC Ensembl
Innerchr9:125055504..125067044hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3811541
hg1911541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117131
Supporting Variants
Samplessample158
Known GenesMRRF
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089750
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