A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110718



Internal ID21293984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131909108..131910965hg38UCSC Ensembl
Innerchr11:131779002..131780859hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv233n145
Supporting Variantsnssv14090921
Samplessample93
Known GenesNTM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110718
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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