A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110739



Internal ID21294005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236659804..236671065hg38UCSC Ensembl
Innerchr1:236823104..236834365hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3811262
hg1911262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n145
Supporting Variantsnssv14094576
Samplessample312
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110739
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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