A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641605



Internal ID6681690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3635433..3638248hg38UCSC Ensembl
Innerchr18:3635433..3638248hg38UCSC Ensembl
Outerchr18:3635198..3638552hg38UCSC Ensembl
chr18:3635432..3638247hg19UCSC Ensembl
Innerchr18:3635432..3638247hg19UCSC Ensembl
Outerchr18:3635197..3638551hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382816
hg192816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15779938, essv15779951, essv15779885, essv15779920, essv15779969, essv15779907, essv15779957, essv15779922, essv15779933, essv15779883, essv15779946, essv15779888, essv15779879, essv15779950, essv15779909, essv15779939, essv15779903, essv15779960, essv15779876, essv15779899, essv15779953, essv15779914, essv15779880, essv15779952, essv15779940, essv15779936, essv15779898, essv15779955, essv15779973, essv15779945, essv15779875, essv15779904, essv15779935, essv15779962, essv15779894, essv15779928, essv15779971, essv15779923, essv15779918, essv15779891, essv15779900, essv15779884, essv15779908, essv15779932, essv15779927, essv15779934, essv15779956, essv15779931, essv15779966, essv15779901, essv15779958, essv15779882, essv15779959, essv15779911, essv15779970, essv15779949, essv15779905, essv15779942, essv15779897, essv15779961, essv15779912, essv15779881, essv15779954, essv15779886, essv15779902, essv15779944, essv15779872, essv15779921, essv15779924, essv15779941, essv15779877, essv15779874, essv15779943, essv15779965, essv15779890, essv15779892, essv15779968, essv15779910, essv15779887, essv15779873, essv15779893, essv15779895, essv15779919, essv15779925, essv15779948, essv15779926, essv15779896, essv15779967, essv15779917, essv15779937, essv15779963, essv15779889, essv15779878, essv15779929, essv15779906, essv15779915, essv15779916, essv15779913, essv15779964, essv15779930, essv15779972, essv15779947
SamplesNA18621, HG00881, HG01813, HG01926, HG02250, HG01440, HG02138, NA18534, NA19310, HG00565, HG01800, NA19072, HG03295, NA19455, HG01845, NA18603, NA18993, HG01085, NA19010, HG02884, HG02105, HG02379, HG02314, HG02389, HG01958, NA18994, HG02322, NA18965, HG03380, HG01841, NA18950, HG02047, HG01812, HG04238, NA18992, HG01392, HG00406, HG02121, NA18622, HG02032, NA18990, HG00689, HG03770, NA18592, NA19083, NA19440, HG01556, NA18976, NA19075, HG00634, HG00982, NA18634, NA18643, HG01599, HG00662, NA18539, HG00867, HG01797, NA19213, NA18747, NA18645, NA19189, NA18954, HG04161, NA19024, NA18558, HG02017, NA18748, NA18942, HG00513, HG01260, HG02384, HG02364, HG02072, NA19091, HG03713, HG02190, NA18543, NA18619, HG00445, HG00611, HG00650, NA18740, HG02351, NA18565, HG01862, HG02035, NA18614, NA19225, HG02678, HG00422, NA19006, HG01855, HG01842, NA18574, HG00473, NA19087, HG01863, HG02396, NA18519, HG02512, NA19439
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641605
Frequency
Sample Size2504
Observed Gain0
Observed Loss102
Observed Complex0
Frequencyn/a


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