A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112852



Internal ID21296118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94596616..94656197hg38UCSC Ensembl
Innerchr11:94329782..94389363hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3859582
hg1959582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090950
Samplessample109
Known GenesPIWIL4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112852
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer