A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550209



Internal ID16337618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22318900..22326562hg38UCSC Ensembl
Innerchr10:22607829..22615491hg19UCSC Ensembl
Innerchr10:22647835..22655497hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg387663
hg197663
hg187663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1003n54
Supporting Variantsnssv744710
Samples
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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