A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669092



Internal ID9588511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74806694..74807065hg38UCSC Ensembl
chr11:74517739..74518110hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5911766, essv6211341
SamplesHG01359, NA18871
Known GenesRNF169
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669092
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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