A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113528



Internal ID21296794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61027801..61031801hg38UCSC Ensembl
Innerchr20:59602857..59606857hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv696n145
Supporting Variantsnssv14099808, nssv14099063, nssv14099920, nssv14099807
Samplessample119, sample198, sample118, sample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113528
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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