A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116297



Internal ID21299563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2865829..2889237hg38UCSC Ensembl
Innerchr6:2866063..2889471hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3823409
hg1923409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083951
Samplessample416
Known GenesMGC39372, SERPINB9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116297
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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