A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664023



Internal ID9583442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82411998..82412107hg38UCSC Ensembl
chr17:80369874..80369983hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5643297, essv5647499, essv6280806, essv5427877, essv6380149, essv5950828, essv5504296, essv5814116, essv6309204, essv6264976, essv5800213, essv5864032, essv5765081, essv5836663, essv6097763, essv6447114, essv6344359, essv6176199, essv6476139, essv6017309, essv5549639, essv6014276, essv6132535, essv5688289, essv6158999, essv5994441, essv6589041, essv6238976, essv5924212, essv6184730, essv6033177, essv5881819, essv5559324, essv6033599, essv5626817, essv6430010, essv5926176, essv6451067, essv5868356, essv6383040, essv6217051, essv6135808, essv5509631, essv6004776, essv6426915, essv5532200, essv6219220, essv5441047, essv6006112, essv5886033, essv5903244, essv6266528, essv6306348, essv5397015, essv5663384, essv5632767, essv5548385, essv6360628, essv5409547, essv6369005, essv6500405, essv6098709, essv5548372, essv6319493, essv6483252, essv5829450, essv6497234, essv6598130, essv6127552, essv6336066, essv5786935, essv6465139, essv5795894, essv5422608, essv6037863, essv5563662, essv5561374, essv6059653, essv5561102, essv5468278, essv6169697, essv6324400, essv6295967, essv6075752, essv5452401, essv5650825, essv6116104, essv6211348, essv6342010, essv6362119, essv5715973
SamplesHG00613, NA18964, HG00619, HG01353, NA18530, HG00418, HG00705, HG00437, HG01083, NA18612, HG00464, NA19072, HG00707, NA18603, HG00657, HG00614, HG00428, NA19010, HG01350, NA18546, NA20588, HG00111, HG00404, HG00319, HG00699, NA18557, NA20586, NA18632, NA19077, HG00154, NA18559, HG00321, HG00556, HG00346, HG01140, HG00472, HG00421, HG00583, NA18622, NA18617, HG00419, NA18547, HG01360, HG00284, HG00237, HG00584, HG00662, HG00436, HG00620, NA18620, HG00653, NA18986, HG00263, HG01069, NA18564, HG00513, NA18988, HG00512, HG01070, NA19074, NA19328, NA19789, HG00589, NA18606, NA18543, NA18582, NA19138, NA19078, HG00650, NA19009, HG00138, HG00663, HG00580, NA18577, NA19064, HG00281, HG00656, HG01366, NA18571, NA18611, HG00324, NA18532, NA18549, HG00442, HG01374, HG00473, HG00137, HG00684, NA18615, HG00704, HG00327
Known GenesOGFOD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664023
Frequency
Sample Size1151
Observed Gain0
Observed Loss91
Observed Complex0
Frequencyn/a


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