A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115702



Internal ID21298968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38814837..38817534hg38UCSC Ensembl
Innerchr21:40186761..40189458hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382698
hg192698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv707n145
Supporting Variantsnssv14102170
Samplessample375
Known GenesETS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115702
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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