A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666053



Internal ID9932158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64010811..64011085hg38UCSC Ensembl
chr11:63778283..63778557hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6338722, essv6201500, essv5667397, essv6513198, essv5731034, essv5692397, essv6544055, essv5863387
SamplesNA19359, NA20291, NA19385, NA19395, NA19401, NA19375, HG01108, NA19360
Known GenesMACROD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666053
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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