A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105382



Internal ID21267468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32623004..32636482hg38UCSC Ensembl
Innerchr3:32664496..32677974hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3813479
hg1913479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112366
Supporting Variants
Samplessample112
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105382
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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