A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107890



Internal ID21280220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36590528..36595494hg38UCSC Ensembl
Innerchr3:36632020..36636986hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg384967
hg194967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113867
Supporting Variants
Samplessample295
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107890
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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