A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620967



Internal ID7007837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86842993..86843364hg38UCSC Ensembl
Innerchr9:86842994..86843364hg38UCSC Ensembl
Outerchr9:86842993..86843365hg38UCSC Ensembl
chr9:89457908..89458279hg19UCSC Ensembl
Innerchr9:89457909..89458279hg19UCSC Ensembl
Outerchr9:89457908..89458280hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13546878, essv13546937, essv13546932, essv13546940, essv13546956, essv13546920, essv13546958, essv13546948, essv13546933, essv13546914, essv13546910, essv13546906, essv13546883, essv13546881, essv13546901, essv13546971, essv13546949, essv13546913, essv13546972, essv13546953, essv13546890, essv13546970, essv13546925, essv13546941, essv13546880, essv13546879, essv13546931, essv13546967, essv13546965, essv13546951, essv13546927, essv13546926, essv13546943, essv13546968, essv13546961, essv13546962, essv13546930, essv13546928, essv13546929, essv13546923, essv13546974, essv13546924, essv13546882, essv13546935, essv13546905, essv13546884, essv13546946, essv13546919, essv13546904, essv13546907, essv13546917, essv13546896, essv13546942, essv13546912, essv13546934, essv13546898, essv13546908, essv13546889, essv13546973, essv13546888, essv13546894, essv13546960, essv13546952, essv13546939, essv13546916, essv13546957, essv13546955, essv13546950, essv13546892, essv13546915, essv13546945, essv13546969, essv13546903, essv13546966, essv13546947, essv13546954, essv13546899, essv13546885, essv13546902, essv13546877, essv13546911, essv13546944, essv13546900, essv13546918, essv13546895, essv13546891, essv13546922, essv13546963, essv13546964, essv13546893, essv13546897, essv13546886, essv13546959, essv13546921, essv13546909, essv13546938, essv13546936, essv13546887
SamplesNA18502, NA19701, HG02702, NA19704, HG02318, HG03115, HG02891, HG02012, HG03280, HG03297, NA19190, NA20356, HG03069, HG03095, NA19446, HG03074, HG03464, NA19379, HG02621, NA19723, NA19131, NA19023, HG03578, HG03224, HG02816, NA20291, HG02922, HG03079, HG02281, HG03209, HG02143, HG03556, NA19372, NA19317, HG03352, NA19189, NA18520, HG02479, HG02439, HG03160, HG03061, NA18934, HG03088, HG02334, HG02582, NA19184, HG03291, NA19455, HG02554, HG02450, HG02508, HG03311, HG01447, HG03085, HG02429, HG03382, HG02817, NA18912, HG03446, HG02309, NA19740, NA19338, HG02666, HG02585, NA18523, HG02332, HG02896, NA18858, HG01956, HG02675, HG01990, HG03567, NA19440, NA19712, NA19434, HG02721, NA19331, HG01958, HG02923, HG02611, NA19334, NA19428, NA19310, NA19360, NA19376, NA19323, NA19117, HG03432, HG02974, HG01556, HG03049, NA19093, HG03060, NA18876, HG02052, HG02763, HG02855, HG02006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620967
Frequency
Sample Size2504
Observed Gain0
Observed Loss98
Observed Complex0
Frequencyn/a


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