A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117199



Internal ID21300465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4313515..4422077hg38UCSC Ensembl
Innerchr20:4294162..4402724hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38108563
hg19108563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099845
Samplessample145
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117199
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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