A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110149



Internal ID21293415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226404441..226413605hg38UCSC Ensembl
Innerchr1:226592142..226601306hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg389165
hg199165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094565
Samplessample312
Known GenesPARP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110149
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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