A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100931



Internal ID21292030
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 StatusS
Merged Variantsnsv3111767
Supporting Variants
Samplessample82
Known GenesFAM3B, MX1, MX2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100931
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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