A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658549



Internal ID9577968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1659736..1659857hg38UCSC Ensembl
chr10:1701930..1702051hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5498846, essv6585210, essv5841510, essv6216071, essv5945494, essv6225170, essv5924801, essv5566048, essv5863486, essv6250106, essv5444259, essv6147385, essv5586470, essv6524650, essv5861937, essv5934368, essv6198853, essv6206407, essv5590743, essv6473862, essv6581070, essv5500970, essv6414228, essv6275788, essv5737075, essv5460469, essv6161755, essv5699346, essv5881503, essv5708328, essv6383368, essv5707562, essv6061086, essv5605804, essv6497794, essv5611314, essv6090773, essv6561349, essv6204135, essv6399970, essv6485149, essv6127907, essv6324412, essv5639655, essv6084197, essv5687215, essv6493195, essv6197742, essv6445411, essv6506389, essv6288859, essv5907221, essv6022786, essv6219191, essv5813683, essv6425347, essv6551453, essv5465207, essv5916622, essv6075191, essv6140555, essv6410097, essv6007962, essv5692605, essv6412964, essv6470568, essv5489983, essv6385831, essv5867577, essv6265835, essv6383150, essv5432953, essv6021941, essv6362550, essv5923030, essv6236642, essv6287852, essv6344150, essv6462620, essv5572541, essv6060072, essv6555725, essv5856340, essv5686023, essv6109342, essv6080384, essv6329614, essv5578885, essv5466550, essv5825386, essv5957870, essv6418041, essv5593423, essv6368089, essv5423559, essv5982190, essv6503138, essv6595527, essv5652887, essv5417948, essv6017722, essv5925658, essv6571467, essv5952854, essv5728700, essv6331135, essv5541877, essv6266468, essv6330660, essv5999641, essv5696033, essv5926088, essv5588282, essv6195833, essv6355386, essv5980172, essv6358310, essv6480363, essv6583329, essv5928852, essv6326523, essv6185481, essv5929189
SamplesHG00323, HG01357, HG00613, NA12827, NA18621, HG00309, HG00313, NA19445, HG00537, NA18605, HG00536, HG00619, NA18534, HG01353, NA18530, HG00418, NA18561, HG00705, HG00437, HG00500, HG01173, NA18612, NA19072, HG00707, HG00463, HG00614, HG01082, HG00428, HG00475, NA20342, HG00326, HG00111, HG00581, HG00280, HG00699, NA18557, HG00353, HG00479, NA18632, HG00543, HG00154, HG01107, NA18559, HG00556, HG00346, HG00472, HG00421, HG00337, HG01378, NA18576, NA18622, NA18623, HG00692, HG01183, HG00689, NA11933, HG00533, NA18609, HG00419, HG00125, NA18637, HG00254, HG00284, NA19457, HG00237, HG00584, HG00662, HG00436, HG00620, HG00108, NA18620, NA18633, NA18572, HG00325, HG00672, HG01069, HG00249, HG00478, NA18613, HG00513, HG00524, HG00512, HG00534, HG00525, NA18562, HG00589, NA18606, NA18543, NA18940, NA18619, NA18582, HG00427, HG00590, HG00443, NA18599, HG00650, HG00663, HG00580, HG00448, NA18602, HG00608, NA20513, HG00530, NA18548, NA11830, NA19749, HG00656, HG01366, HG00422, HG00708, HG01108, HG00693, HG00275, NA18532, HG00442, HG00473, HG01377, HG00476, HG00671, NA19087, HG00702, HG00704, HG00271
Known GenesADARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658549
Frequency
Sample Size1151
Observed Gain0
Observed Loss123
Observed Complex0
Frequencyn/a


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