A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112740



Internal ID21296006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55799073..55820667hg38UCSC Ensembl
Innerchr8:56711632..56733226hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3821595
hg1921595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088234
Samplessample385
Known GenesTGS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112740
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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