A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550207



Internal ID15990930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22316183..22342327hg38UCSC Ensembl
Innerchr10:22605112..22631256hg19UCSC Ensembl
Innerchr10:22645118..22671262hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3826145
hg1926145
hg1826145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744708
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)nsv550207
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer