A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668102



Internal ID9587521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27752542..27752689hg38UCSC Ensembl
chr10:28041471..28041618hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5926180, essv5890471, essv6520334, essv6551003, essv5486853, essv6215800, essv6150163, essv6572637, essv5937138, essv5582435, essv5522549, essv5412631, essv6297149, essv5492541, essv5747931, essv5546520, essv5760015, essv5638261, essv6321791, essv6391070, essv6239042, essv5945143, essv6078967, essv5463742, essv5553604, essv6531823, essv6471245, essv5582063, essv6213726, essv6143451, essv6329733, essv6469269, essv6100674, essv6180999, essv5734290, essv5892795, essv6548821, essv5588882, essv6556420, essv6162116, essv5705934, essv6581011, essv6573755, essv5571208, essv6071843, essv6473394, essv5460220, essv6264203, essv5523516, essv6009976, essv6244565, essv6350790, essv5779249, essv5954309, essv5655124, essv5721912, essv5822932, essv5903053, essv6571385, essv6045543, essv6400593, essv6392861, essv6264382, essv6268367, essv6315663, essv6528811, essv5729344, essv5441003, essv5931724, essv5847066, essv6106535, essv6450839, essv5439296, essv5788544
SamplesHG00613, NA19012, NA18964, HG00313, HG00537, HG00607, NA18534, NA18530, HG00418, NA18561, NA18612, NA18550, NA18603, HG00657, NA18953, HG01488, NA18608, NA18541, NA18546, NA19685, NA18557, NA18943, NA18628, NA19054, NA19057, NA19068, NA18576, NA18960, NA18618, HG01061, HG00330, NA19066, NA18547, NA18634, HG00584, NA18572, HG00325, NA18986, HG00501, HG00672, HG01069, HG00513, HG00524, NA18988, HG00512, HG01070, HG00525, NA18985, HG00589, NA18543, NA18999, NA18552, NA18567, NA18989, HG00580, NA18544, NA18577, NA18944, NA19063, HG00422, HG00708, NA18984, NA18611, HG01177, HG00625, NA18549, NA19079, HG00684, HG00671, HG00704, NA18555, NA19065, HG00531, NA18553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668102
Frequency
Sample Size1151
Observed Gain0
Observed Loss74
Observed Complex0
Frequencyn/a


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