A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111767



Internal ID21295033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41339601..41441695hg38UCSC Ensembl
Innerchr21:42711528..42813622hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38102095
hg19102095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100931
Samplessample82
Known GenesFAM3B, MX1, MX2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111767
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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