A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1003n54



Internal ID22768898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22318503..22326834hg38UCSC Ensembl
chr10:22607432..22615763hg19UCSC Ensembl
chr10:22647438..22655769hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg388332
hg198332
hg188332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550208, nsv550209
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)dgv1003n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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