A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660994



Internal ID9927099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32510927..32548603hg38UCSC Ensembl
chr6:32478704..32516380hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3837677
hg1937677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1104e199
Supporting Variantsessv6332012, essv5474711, essv6242208, essv6426742, essv6200349, essv5448074, essv6427499, essv6080948, essv5815831, essv5784948, essv6098026, essv5534215, essv6400138, essv6585146, essv5987666, essv6220014, essv5453610, essv6190923, essv5424285, essv5654582, essv5629154, essv5466425, essv6232216, essv5686401, essv6553592, essv6367818, essv5751902, essv6330328, essv6385829, essv5462656, essv5969124, essv5871857, essv5628044, essv5489136, essv5748543, essv6465478, essv5852002, essv6041294, essv5412818, essv6199259, essv5948471, essv5409899, essv5792222, essv6020817, essv5675245, essv6089802, essv5953831, essv6285185, essv5905907, essv5734214, essv6426517, essv6558804, essv6507914, essv5587309, essv6259382, essv6075460, essv5409794, essv6384900, essv6137163, essv5866151, essv5756967, essv5885676, essv6267099, essv5705400, essv6381020, essv6185905, essv6158339, essv6552727, essv6006425, essv6365185, essv6161172, essv6341959, essv5497512, essv6100778, essv6496368, essv5474949, essv6419420, essv6193911, essv6099792, essv6093791, essv5750494, essv6364830, essv5700669, essv6171674, essv6536204, essv6200419, essv5535919, essv5396624, essv5670544, essv5943957
SamplesNA19394, NA12717, NA11830, NA18508, HG01359, NA19399, NA18980, NA18507, NA20816, NA18486, NA19393, HG00449, HG00177, NA19190, HG00337, HG00327, NA20814, NA20796, NA19379, NA18944, HG00448, NA20795, NA20769, NA18547, NA18942, NA20768, NA18498, NA20541, HG00281, NA12275, NA19383, HG00335, NA20819, HG00325, NA12044, HG00427, NA20811, NA19189, HG00338, NA18973, HG00419, NA19921, HG00133, HG01136, NA18605, NA18613, HG01187, NA19391, NA18516, NA20506, NA18579, NA18566, HG00284, HG00273, NA12829, HG00321, NA19225, NA20828, NA18523, NA18536, NA19625, NA20765, HG00258, NA20773, NA19390, NA19147, NA18559, NA18517, NA12775, NA20804, HG00278, NA20520, NA20530, NA20778, NA19470, NA19428, NA20544, NA19467, HG00116, NA20516, NA19360, NA19398, NA18501, HG00656, NA19713, NA19129, HG00345, NA20585, NA18522, NA19431
Known GenesHLA-DRB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660994
Frequency
Sample Size1151
Observed Gain0
Observed Loss90
Observed Complex0
Frequencyn/a


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