A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2889n54



Internal ID22770784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114531958..114568632hg38UCSC Ensembl
chr12:114969763..115006437hg19UCSC Ensembl
chr12:113454146..113490820hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3836675
hg1936675
hg1836675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560294, nsv560293
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2889n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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