A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110601



Internal ID21293867
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 StatusM
Merged Variants
Supporting Variantsnssv14089716
Samplessample145
Known GenesCDK5RAP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110601
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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