A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110752



Internal ID21294018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65142617..65143315hg38UCSC Ensembl
Innerchr16:65176520..65177218hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n145
Supporting Variantsnssv14098425, nssv14099205, nssv14096438
Samplessample182, sample112, sample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110752
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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