A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117566



Internal ID21300832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19019387..19022883hg38UCSC Ensembl
Innerchr21:20391706..20395202hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv697n145
Supporting Variantsnssv14100944, nssv14100894
Samplessample41, sample96
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117566
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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