A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5542779



Internal ID9581257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1522128..1522902hg38UCSC Ensembl
chr11:1543358..1544132hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665572
Supporting Variants
SamplesNA19160
Known GenesMOB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5542779
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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