A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112337



Internal ID21295603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163971946..164020009hg38UCSC Ensembl
Innerchr3:163689734..163737797hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3848064
hg1948064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv820n145
Supporting Variantsnssv14108326
Samplessample235
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112337
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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