A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091103



Internal ID21289778
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 StatusS
Merged Variantsnsv3112365
Supporting Variants
Samplessample51
Known GenesCCDC73, PRRG4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091103
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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