A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113083



Internal ID21296349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131909126..131910965hg38UCSC Ensembl
Innerchr11:131779020..131780859hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv233n145
Supporting Variantsnssv14091132, nssv14091135
Samplessample62, sample64
Known GenesNTM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113083
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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