A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088535



Internal ID21273239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22322698..22326943hg38UCSC Ensembl
Innerchr10:22611627..22615872hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384246
hg194246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116796
Supporting Variants
Samplessample189
Known GenesBMI1, COMMD3-BMI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088535
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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