A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104295



Internal ID21289614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32621583..32627425hg38UCSC Ensembl
Innerchr3:32663075..32668917hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385843
hg195843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110578
Supporting Variants
Samplessample49
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104295
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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