A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113045



Internal ID21296311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17957518..17959735hg38UCSC Ensembl
Innerchr20:17938162..17940378hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382218
hg192217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100711
Samplessample331
Known GenesSNX5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113045
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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