A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108548



Internal ID21284079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180313691..180318570hg38UCSC Ensembl
Innerchr3:180031479..180036358hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384880
hg194880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115865
Supporting Variants
Samplessample357
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108548
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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