A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112365



Internal ID21295631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32794060..32865419hg38UCSC Ensembl
Innerchr11:32815606..32886965hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3871360
hg1971360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091103
Samplessample51
Known GenesCCDC73, PRRG4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112365
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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