A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090151



Internal ID21269329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22322794..22324966hg38UCSC Ensembl
Innerchr10:22611723..22613895hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg382173
hg192173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110257
Supporting Variants
Samplessample138
Known GenesBMI1, COMMD3-BMI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090151
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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