A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113695



Internal ID21296961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19019387..19023283hg38UCSC Ensembl
Innerchr21:20391706..20395602hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383897
hg193897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv697n145
Supporting Variantsnssv14102022
Samplessample213
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113695
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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