A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117287



Internal ID21300553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46660183..46670990hg38UCSC Ensembl
Innerchr21:48080095..48090902hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810808
hg1910808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102033
Samplessample224
Known GenesPRMT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117287
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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