A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628005



Internal ID7014830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126365411..126381998hg38UCSC Ensembl
chr11:126235306..126251893hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3816588
hg1916588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv235e214
Supporting Variantsessv14302971, essv14302970, essv14302982, essv14302967, essv14302981, essv14302973, essv14302988, essv14302975, essv14302983, essv14302991, essv14302974, essv14302987, essv14302986, essv14302984, essv14302972, essv14302989, essv14302990, essv14302976, essv14302980, essv14302977, essv14302985, essv14302968, essv14302979, essv14302969, essv14302978
SamplesHG02890, HG02702, HG02895, NA19201, HG01953, HG02595, NA07048, HG03246, HG03224, HG02562, HG03460, HG03054, HG01889, HG02568, HG02772, HG02813, HG02557, HG02839, HG03473, HG02771, HG03432, HG03039, NA20852, HG02465, HG02808
Known GenesST3GAL4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628005
Frequency
Sample Size2504
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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