A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12869n54



Internal ID22780764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126610956..126701334hg38UCSC Ensembl
chr9:129373235..129463613hg19UCSC Ensembl
chr9:128413056..128503434hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3890379
hg1990379
hg1890379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615315, nsv615314
Samples
Known GenesLMX1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12869n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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