A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089716



Internal ID21269944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120390239..120395643hg38UCSC Ensembl
Innerchr9:123152517..123157921hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110601
Supporting Variants
Samplessample145
Known GenesCDK5RAP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089716
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