A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110609



Internal ID21293875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72834846..72836534hg38UCSC Ensembl
Innerchr16:72868745..72870433hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg381689
hg191689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n145
Supporting Variantsnssv14098242
Samplessample23
Known GenesZFHX3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110609
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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