A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625566



Internal ID7012400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21135401..21286053hg38UCSC Ensembl
chr11:21156947..21307599hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38150653
hg19150653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14047486, essv14047479, essv14047476, essv14047477, essv14047506, essv14047507, essv14047496, essv14047475, essv14047468, essv14047470, essv14047494, essv14047503, essv14047501, essv14047504, essv14047490, essv14047491, essv14047505, essv14047489, essv14047466, essv14047469, essv14047487, essv14047498, essv14047499, essv14047472, essv14047478, essv14047481, essv14047484, essv14047464, essv14047465, essv14047474, essv14047508, essv14047485, essv14047462, essv14047488, essv14047500, essv14047502, essv14047497, essv14047467, essv14047480, essv14047473, essv14047495, essv14047483, essv14047493, essv14047492, essv14047482, essv14047471, essv14047463, essv14047461
SamplesHG02944, HG02628, NA19397, NA19393, HG03297, HG03069, HG02769, HG03095, NA19379, HG03168, NA19307, HG02325, HG02885, NA19235, NA19207, HG03352, NA19209, HG03114, HG02477, HG02977, NA19437, HG01171, HG02582, NA19347, HG02144, HG03575, HG01390, HG01161, NA19225, HG02675, NA19017, HG03437, NA19434, NA19454, NA19144, HG03433, HG02317, NA19360, NA19376, NA19117, HG01912, NA19472, HG03049, HG02462, NA19312, HG02808, NA19214, NA19153
Known GenesNELL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625566
Frequency
Sample Size2504
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer