A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113195



Internal ID21296461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5888233..5894343hg38UCSC Ensembl
Innerchr18:5888232..5894342hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv509n145
Supporting Variantsnssv14100961
Samplessample404
Known GenesTMEM200C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113195
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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