A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2666569

Internal ID9585988
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124339599..124339731hg38UCSC Ensembl
chr12:124824145..124824277hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5845703, essv5617888, essv5831790, essv6201450, essv6244227, essv6415815, essv5802585, essv5737402, essv5443251, essv5507232, essv6085280, essv6328525, essv5496728, essv5535972, essv6038555, essv6176110, essv6357670, essv6536071, essv6205188, essv5991265, essv6486121, essv5725614, essv5782026, essv5980420, essv6171577, essv6353757, essv5502922, essv5873877, essv6035408, essv5539486, essv5839062, essv5559908, essv5523343, essv5618176, essv5856935, essv5531968, essv5433269, essv6077975, essv6272940, essv5630264, essv5683532, essv6250120, essv5626693, essv6267052, essv6009852, essv6032525, essv5911831, essv6384054, essv5677057, essv6165561, essv6216505, essv6391667, essv5786424, essv6576559, essv6192025, essv6535249, essv5439028, essv5720802, essv6265402, essv6087093, essv6521442, essv6282314, essv6442716, essv6224457, essv6289276, essv5511790, essv6333261, essv5880956, essv6391421, essv5606859, essv6044244, essv5678475, essv5482359, essv6337391, essv5806648, essv5721372, essv6021437, essv6212753, essv5528543, essv5408761, essv6008837, essv6559506, essv6379543, essv5963460, essv6038282, essv6216102, essv6059188, essv5933074, essv5452437, essv5889695, essv6378952, essv5582820, essv6444343, essv6179730, essv5892383, essv6534003, essv6557248, essv5676078, essv6155568, essv5886231, essv6406245, essv5753869, essv5422104, essv5611629, essv5442507, essv5880708, essv5795378, essv5503883, essv5499634, essv5631987, essv5771534, essv6497427, essv5876937, essv5471694, essv5831904, essv6537322, essv6326897, essv5829178, essv5993768
SamplesHG00613, NA12827, NA19625, NA12249, NA18861, HG00252, NA12748, NA11930, NA07037, NA20809, HG00619, HG00418, HG01072, NA19404, HG00328, NA18952, HG00437, HG01173, NA20796, HG00449, NA18570, NA18545, NA18603, NA18948, HG00657, NA18516, NA19317, NA20800, HG01082, NA20816, NA12828, HG00375, NA20342, NA20778, HG01350, HG00701, HG00698, HG00111, HG00280, HG00253, NA12044, NA18632, HG00154, HG01107, HG00339, NA19428, NA19383, HG00346, HG01384, NA12282, NA20515, HG00421, NA12004, NA18566, HG00337, NA11994, NA18536, NA18576, HG00372, NA20801, HG00315, NA12761, NA11933, NA18609, NA20765, HG00125, NA11831, NA12829, NA18637, HG00254, HG00276, HG01187, NA12830, HG00237, NA19324, NA20773, NA12006, HG00373, HG00108, NA18572, NA20760, NA12778, NA19373, HG00629, HG00185, HG00239, HG00672, HG01069, NA20818, NA18613, NA20542, NA18606, NA18543, NA18582, NA18597, NA20537, HG00650, HG00663, NA19099, NA20507, NA12003, HG00281, NA12842, HG01366, HG01108, HG01251, HG00693, NA11932, HG00320, HG00137, NA20804, NA20806, HG01377, NA19758, HG00345, NA18555, HG00278, HG00136, NA12775
Known GenesNCOR2
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2666569
Sample Size1151
Observed Gain0
Observed Loss119
Observed Complex0

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