A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112906



Internal ID21296172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71988951..72001153hg38UCSC Ensembl
Innerchr3:72038102..72050304hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3812203
hg1912203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108089
Samplessample336
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112906
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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