A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114918



Internal ID21298184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19020759..19022769hg38UCSC Ensembl
Innerchr21:20393078..20395088hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv698n145
Supporting Variantsnssv14100942, nssv14102166, nssv14102017, nssv14101954, nssv14100877
Samplessample93, sample28, sample209, sample152, sample372
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114918
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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