A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113213



Internal ID21296479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72834646..72836414hg38UCSC Ensembl
Innerchr16:72868545..72870313hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg381769
hg191769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n145
Supporting Variantsnssv14096556, nssv14096451
Samplessample360, sample292
Known GenesZFHX3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113213
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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