A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115409



Internal ID21298675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131909108..131910292hg38UCSC Ensembl
Innerchr11:131779002..131780186hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091039, nssv14090915
Samplessample92, sample138
Known GenesNTM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115409
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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