A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110835



Internal ID21294101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10720396..10726234hg38UCSC Ensembl
Innerchr12:10872995..10878833hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg385839
hg195839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093889
Samplessample397
Known GenesYBX3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110835
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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