A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111062



Internal ID21294328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:216592604..216596325hg38UCSC Ensembl
Innerchr2:217457327..217461048hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg383722
hg193722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102456
Samplessample49
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111062
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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