A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114441



Internal ID21297707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23666919..23677764hg38UCSC Ensembl
Innerchr3:23708410..23719255hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3810846
hg1910846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107094
Samplessample266
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114441
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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