A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117151



Internal ID21300417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6023658..6094457hg38UCSC Ensembl
Innerchr11:6044888..6115687hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3870800
hg1970800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091099
Samplessample49
Known GenesOR56A1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117151
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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