A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1675n54



Internal ID22769570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18919563..18942188hg38UCSC Ensembl
chr11:18941110..18963735hg19UCSC Ensembl
chr11:18897686..18920311hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822626
hg1922626
hg1822626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553636, nsv553638, nsv553637
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1675n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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