A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106450



Internal ID21270314
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 StatusS
Merged Variantsnsv3117443
Supporting Variants
Samplessample149
Known GenesROBO2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106450
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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