A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660528



Internal ID9926633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5763186..5787892hg38UCSC Ensembl
Outerchr11:5762715..5788262hg38UCSC Ensembl
Innerchr11:5784416..5809122hg19UCSC Ensembl
Outerchr11:5783945..5809492hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825548
hg1925548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv189e199
Supporting Variantsessv6239856, essv5720720, essv6272916, essv5769261, essv6558220, essv6014962, essv5551883, essv6211353, essv6340524, essv6423050, essv5620343, essv6265190, essv6448515, essv6435917, essv6385986, essv6337811, essv5678426, essv6384473, essv5919799, essv5543510, essv5430999, essv6542997, essv5876415, essv5905804, essv5852566, essv5551109, essv6026750, essv5927208, essv6108776, essv5438325, essv6259855, essv5958994, essv6089201, essv6193108, essv5879636, essv5806721, essv5499382, essv5713123, essv5956530, essv6348213
SamplesHG01060, HG01098, HG01462, HG01374, HG01066, HG01456, HG00737, HG01140, HG01250, HG01351, HG01488, HG00736, HG01354, HG01083, HG01365, HG01134, HG01080, HG01067, HG01124, HG01353, HG01183, HG00731, HG01187, HG01171, HG01384, HG01197, HG01101, HG01107, HG01204, HG01075, HG01148, HG01253, HG01113, HG01137, HG01108, HG01254, HG01251, HG01097, HG00554, HG01061
Known GenesOR52N1, OR52N5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660528
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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