A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550206



Internal ID15990929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22314389..22327341hg38UCSC Ensembl
Innerchr10:22603318..22616270hg19UCSC Ensembl
Innerchr10:22643324..22656276hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3812953
hg1912953
hg1812953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1002n54
Supporting Variantsnssv744707
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)nsv550206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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