A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106441



Internal ID21270131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193742750..193747288hg38UCSC Ensembl
Innerchr3:193460539..193465077hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg384539
hg194539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113821
Supporting Variants
Samplessample147
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106441
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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