A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672889



Internal ID9592308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87989681..87989918hg38UCSC Ensembl
chr16:88023287..88023524hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5418185, essv6284095, essv5739735, essv6346905, essv6418363, essv5966623, essv5484842, essv6325623, essv6454995, essv6370679, essv6016524, essv6141475, essv6379710, essv5489506, essv5960978, essv6378691, essv5639719, essv6509392, essv5758382, essv6113232, essv6095658, essv5506920, essv5516812, essv5863698, essv5543003, essv6478905, essv6282769, essv6157717, essv6566754, essv5673064, essv5535317, essv5512280, essv6451813, essv5699898, essv5806099, essv5775247, essv5495888, essv5423077, essv5962690, essv6550393, essv6068659, essv5919092, essv6337456, essv6216914, essv6224591, essv6162919, essv5405131, essv5732341, essv5828890, essv5717111, essv6003638, essv5519936, essv6247312, essv5847577, essv6544651, essv5758573, essv5541886, essv6220705, essv5796960, essv5484309, essv6391451, essv5452917, essv6130330, essv5561217, essv5925232, essv5561058, essv6098782, essv5406257, essv6148594, essv6440176, essv5729831, essv5824299, essv6102795, essv6511789, essv5901702, essv5890041, essv5941301, essv6208456, essv5730047, essv5490550, essv5999201, essv6146607, essv5722863, essv6136303, essv6533532, essv5855606, essv5525723, essv5944801, essv5921470, essv5540788, essv5837359, essv5769760, essv6029936, essv6006938, essv5540527, essv6058202
SamplesNA18621, HG00537, HG01440, NA18534, HG01353, NA18530, NA19819, HG01055, HG00705, HG00500, HG01173, NA18612, HG00464, HG00131, HG00707, HG00463, HG00657, HG00614, HG01365, HG00475, HG00542, HG01174, NA18546, HG00701, HG00683, HG01188, HG00581, HG00280, HG01101, HG00319, NA18557, HG01171, NA18596, HG00342, HG00543, HG01107, NA18559, HG01375, HG00421, HG00583, NA18635, NA18536, HG01048, HG00692, HG01047, NA18636, HG00315, HG00533, HG00419, HG00125, NA18637, HG01187, HG00237, HG00584, HG00662, HG00620, HG01437, NA18633, HG00653, HG01066, NA18558, HG00501, HG00672, HG00478, HG01351, HG00740, NA18613, HG00513, HG00524, HG00512, HG00534, HG00246, HG00589, NA18606, NA18543, HG00427, HG00443, NA18599, HG00650, HG00448, NA18602, HG00608, HG01390, HG00422, HG01108, HG00693, NA18611, NA18549, HG00442, HG00684, HG00476, HG00704, HG00271, HG00531, HG01067, HG00327
Known GenesBANP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672889
Frequency
Sample Size1151
Observed Gain0
Observed Loss96
Observed Complex0
Frequencyn/a


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