A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2672889

Internal ID9592308
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87989681..87989918hg38UCSC Ensembl
chr16:88023287..88023524hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2672889
Sample Size1151
Observed Gain0
Observed Loss96
Observed Complex0

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