A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088693



Internal ID21278036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22314287..22327757hg38UCSC Ensembl
Innerchr10:22603216..22616686hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3813471
hg1913471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115866
Supporting Variants
Samplessample263
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088693
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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