A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663106



Internal ID9929211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154517582..154519388hg38UCSC Ensembl
Outerchr6:154517211..154519758hg38UCSC Ensembl
Innerchr6:154838716..154840522hg19UCSC Ensembl
Outerchr6:154838345..154840892hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5866172, essv6065300, essv6058864, essv6040442, essv5889992, essv5688496, essv6132799, essv6357580, essv5826254, essv5967626, essv5808739, essv6182898, essv6222165, essv6139954, essv5605190, essv5532109, essv5992558, essv5896721, essv6083678, essv5870703, essv6187540, essv5812538, essv6445115, essv6588443, essv5731663, essv6145537, essv6213583, essv5822551, essv6189347, essv5969543, essv5752363, essv5836483, essv5533108, essv6123535, essv5434061, essv6574023, essv5723312, essv6219676, essv5754524, essv6477396, essv5937803, essv5906286, essv5674496, essv6452003, essv5821155, essv5929573, essv6013851, essv6508221, essv5831731, essv6182206, essv5680364, essv6269535, essv5821791, essv6372043, essv6314095, essv5408997, essv5756742, essv6033870, essv6318368, essv5577116, essv5398881, essv5450654, essv6129720, essv6186726, essv6596867, essv6233838, essv6525415, essv6168756, essv5771341, essv6185186, essv6567367, essv5626244, essv6482202, essv6039024, essv5935878, essv6235935, essv5740181, essv5494174, essv6084725
SamplesHG00403, HG00650, HG00542, HG00442, HG00536, HG00608, HG00671, HG00524, HG00699, HG00449, HG00654, HG00693, HG00663, HG00589, HG00501, HG00702, HG00689, HG00448, HG00610, HG00537, HG00590, HG00512, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00443, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00651, HG00690, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00580, HG00473, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00472, HG00628, HG00437, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663106
Frequency
Sample Size1151
Observed Gain0
Observed Loss79
Observed Complex0
Frequencyn/a


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