A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113453



Internal ID21296719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118084063..118158591hg38UCSC Ensembl
Innerchr11:117954778..118029306hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3874529
hg1974529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090306
Samplessample419
Known GenesSCN4B, TMPRSS4, TMPRSS4-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113453
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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