A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082877



Internal ID21280803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:269534..360515hg38UCSC Ensembl
Innerchr6:269534..360515hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3890982
hg1990982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110329
Supporting Variants
Samplessample302
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082877
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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