A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625098



Internal ID7011937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1041593..1083882hg38UCSC Ensembl
chr11:1041593..1081878hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3842290
hg1940286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992199
SamplesHG03830
Known GenesMUC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625098
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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