A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110136



Internal ID21293402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13257364..13411138hg38UCSC Ensembl
Innerchr16:13351221..13504995hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38153775
hg19153775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096377
Samplessample251
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110136
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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