A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669097



Internal ID9588516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55596950..55676530hg38UCSC Ensembl
Outerchr11:55596916..55676565hg38UCSC Ensembl
Innerchr11:55364426..55444006hg19UCSC Ensembl
Outerchr11:55364392..55444041hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3879650
hg1979650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv211e199
Supporting Variantsessv5413156
SamplesHG00359
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669097
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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