A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669558



Internal ID9935663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60329949..60330467hg38UCSC Ensembl
chr11:60097422..60097940hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5707829, essv5985767, essv6176039, essv6068189, essv6579605, essv6538810, essv5776813, essv6093908, essv5790402, essv5810818, essv5408970, essv5927004, essv6581280, essv5624027, essv5619555, essv6449409, essv6309151, essv6378647, essv6255881, essv5543728, essv5982319, essv5704998, essv6273746, essv6046706, essv6323903, essv6401023, essv6313379, essv5748986, essv5908186, essv6022739, essv6457835, essv5539817, essv6557428, essv6008563, essv5589150, essv6144103, essv5511213, essv5595162, essv5857437, essv5468198, essv6314141, essv6182780, essv6132412, essv6389220, essv5738449, essv5690109, essv5571453, essv6220370, essv5860032, essv5498022, essv6544380, essv5981869, essv6362224, essv5520133, essv5673906, essv5921153, essv6061388, essv5963183, essv5795108, essv6434963, essv5625438, essv6123515, essv6179919, essv6189426, essv6080532, essv6503778, essv5829509, essv6394781, essv6218096, essv6034025
SamplesNA19394, HG00650, HG00442, NA19700, HG00231, HG00671, HG00242, HG00559, NA19399, NA19332, NA18565, HG01066, NA19350, NA19377, NA18530, NA19190, HG00693, NA19374, NA19373, NA18550, NA18595, NA18635, NA18619, HG00736, NA07347, HG01083, HG00590, HG00158, NA18977, NA19075, NA19471, HG01440, HG00530, HG00419, HG00108, HG01136, NA18544, HG00629, HG00282, NA19077, HG00428, NA19455, HG00436, HG00500, HG01149, NA18534, HG00692, HG00324, NA19461, HG00404, HG01383, HG00613, NA19009, HG00704, HG00141, NA19395, NA18576, HG00258, HG00625, NA19083, HG00707, HG00259, NA19468, NA19080, NA19213, NA18552, HG00595, HG00437, NA19676, HG00593
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669558
Frequency
Sample Size1151
Observed Gain0
Observed Loss70
Observed Complex0
Frequencyn/a


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