A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668092



Internal ID9587511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89362422..89362478hg38UCSC Ensembl
Outerchr14:89362051..89362848hg38UCSC Ensembl
Innerchr14:89828766..89828822hg19UCSC Ensembl
Outerchr14:89828395..89829192hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5876236, essv5874267, essv5812982, essv5641973, essv6217924, essv5966213, essv5763808, essv6596592, essv6025566, essv6184295, essv5934842, essv6060918, essv5902423, essv5908890, essv6094636, essv6592782, essv5624474, essv6334117, essv5862722, essv5804141, essv6329819, essv5569418, essv6057403, essv5976641, essv6406885, essv5988882, essv6542810, essv6158328, essv6247382, essv6505382, essv6524690, essv5504733, essv5775310, essv6171203, essv5668065, essv6205985, essv6106141, essv5931472, essv5962329, essv5690060, essv5406652, essv5668194, essv6500013, essv6032478, essv5874941, essv5965337, essv5929819, essv6462019, essv6088101, essv5627113, essv5645685, essv5538599, essv5930989, essv6008094, essv6329248, essv5992523, essv6408138, essv6133942, essv5768764, essv5851121, essv5646128, essv6421452, essv5546071, essv5990547, essv5498205, essv6408954, essv6543164, essv5682674, essv5802085, essv5629788, essv5855318, essv5690148, essv6090190, essv6466061, essv5985672, essv5808510, essv6329015, essv6548494, essv6334248, essv5703619, essv6289821, essv5748745, essv6030595, essv5549745, essv5892925, essv6222269, essv6524984, essv6198032, essv6333071, essv5475097, essv6128346, essv6228298, essv6074667, essv5679656, essv5857423, essv6219737, essv6488878, essv5588438, essv5579394, essv6235746
SamplesHG01441, NA19012, NA18964, NA18951, NA19081, NA18952, NA18975, NA19060, NA19003, NA19072, NA18948, HG01492, NA18953, NA18972, NA18947, NA19010, NA18963, NA19004, NA18965, NA19084, NA18943, NA18950, HG01171, HG00353, NA18596, NA18949, NA19077, HG00154, NA19062, HG01148, NA19067, NA19085, NA18967, NA19054, NA19059, NA19076, NA19057, NA19068, NA18536, NA18960, NA18990, NA19083, NA19088, NA18956, NA19066, NA18959, NA18976, NA18637, NA18973, NA19075, NA18982, NA19056, NA19082, NA19000, NA19055, NA19380, NA19080, NA19373, NA19384, NA18968, NA18986, NA19005, NA19002, NA18977, NA18941, NA18942, NA18961, NA18988, HG01070, NA19074, NA18910, NA18974, NA18985, NA19462, NA18945, NA18606, NA18940, NA18987, NA18999, NA18983, NA19078, NA19009, NA18989, NA18971, NA19755, NA19064, NA18944, NA19063, NA19070, NA18984, HG00693, NA11829, NA18981, NA19079, NA19087, NA19007, NA19065, NA19058, NA18980, HG01354
Known GenesFOXN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668092
Frequency
Sample Size1151
Observed Gain0
Observed Loss100
Observed Complex0
Frequencyn/a


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