A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1002n54



Internal ID20134426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22313047..22327855hg38UCSC Ensembl
chr10:22601976..22616784hg19UCSC Ensembl
chr10:22641982..22656790hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3814809
hg1914809
hg1814809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550206, nsv550205, nsv550204
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)dgv1002n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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