A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2660474

Internal ID9579893
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85541131..85541452hg38UCSC Ensembl
chr4:86462284..86462605hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6434042, essv5686866, essv5688329, essv5421554, essv6232449, essv5490236, essv6141498, essv5670356, essv5820494, essv5524503, essv6185803, essv6056115, essv6551022, essv5941056, essv5994788, essv5434733, essv6560594, essv5829117, essv6012802, essv5908708, essv5914920, essv6404507, essv6291885, essv5990368, essv6204106, essv5833448, essv6396963, essv6077666, essv5554727, essv5960235, essv6194814, essv6097202, essv5821714, essv6545765, essv5732140, essv5663480, essv5565242, essv5832680, essv6448746, essv6010375, essv6137960, essv6574334, essv6095418, essv5627670, essv6032452, essv6423217, essv6177037, essv6069472, essv5879908, essv6345029, essv6190157, essv6432321, essv6062680, essv6399583, essv6442931, essv5642789, essv5877692, essv5434923, essv6104724, essv6459708, essv6539552, essv5540780, essv5494828, essv6372845, essv5781904, essv6445033, essv6132965, essv6429649, essv6412872, essv5455298, essv6371740, essv6385378, essv5435119, essv6212170, essv5970708, essv6523199, essv6251860, essv5902223, essv5612286, essv5673898, essv5427799, essv5617183, essv6557285, essv6399077, essv6067476, essv6150121, essv6020013, essv6268824, essv5961477, essv5992363, essv6582597, essv5493392, essv5988959, essv5585505, essv5835923, essv5588614, essv6200004, essv5403724, essv5813949, essv6078408, essv6138727, essv6546240, essv5474484, essv6033598, essv5990025, essv6256238
SamplesHG01441, NA20281, NA18870, NA19312, HG00734, NA18861, NA19712, NA18520, NA18595, NA19904, HG01353, NA18523, NA18874, NA19093, NA19311, NA19469, NA18511, NA19359, NA19331, HG01082, NA18517, NA19338, HG00326, NA19920, NA20786, HG01350, NA19461, NA19379, NA18507, HG01188, NA19257, NA19108, NA19355, NA19147, NA18868, NA20340, NA19463, NA19914, NA19383, NA18934, NA18508, NA19239, NA12383, HG00259, NA19444, NA19396, NA19397, NA19398, NA19440, NA19908, NA18973, NA18916, NA19457, NA20341, NA19213, NA19360, NA19313, NA19377, NA19395, NA19189, NA19372, HG01191, NA19374, NA19703, NA19393, NA18498, NA18923, NA19102, NA18522, NA19238, NA20344, NA18502, NA19657, NA19901, NA18504, NA19704, NA19707, NA18910, NA19711, NA19921, NA19138, HG01095, NA19391, NA20276, NA19394, NA19116, NA20289, NA19434, NA19099, NA19452, NA19225, NA18917, NA19399, NA18499, NA18924, NA19371, HG01108, NA19315, NA19130, HG01177, NA19240, NA18853, HG01102, NA19381, HG01110, NA19448
Known GenesARHGAP24
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2660474
Sample Size1151
Observed Gain0
Observed Loss106
Observed Complex0

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