A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660474



Internal ID9579893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85541131..85541452hg38UCSC Ensembl
chr4:86462284..86462605hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38322
hg19322
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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660474
Frequency
Sample Size1151
Observed Gain0
Observed Loss106
Observed Complex0
Frequencyn/a


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