A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082883



Internal ID21280868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296068..382543hg38UCSC Ensembl
Innerchr6:296068..382543hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3886476
hg1986476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112774
Supporting Variants
Samplessample303
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082883
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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