A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2664023

Internal ID9583442
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82411998..82412107hg38UCSC Ensembl
chr17:80369874..80369983hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2664023
Sample Size1151
Observed Gain0
Observed Loss91
Observed Complex0

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