A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117443



Internal ID21300709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77162144..77166029hg38UCSC Ensembl
Innerchr3:77211295..77215180hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383886
hg193886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108168, nssv14106450
Samplessample149, sample208
Known GenesROBO2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117443
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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