A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112067



Internal ID21295333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84699095..84701730hg38UCSC Ensembl
Innerchr16:84732701..84735336hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382636
hg192636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv470n145
Supporting Variantsnssv14098261
Samplessample33
Known GenesUSP10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112067
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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