A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102033



Internal ID21275594
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 StatusS
Merged Variantsnsv3117287
Supporting Variants
Samplessample224
Known GenesPRMT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102033
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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