A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665923



Internal ID9932028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3469442..3469632hg38UCSC Ensembl
chr16:3519442..3519632hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6088841, essv6497848, essv6116887, essv5483462, essv5820228, essv5833264, essv6417162, essv6049304, essv6572601, essv5976788, essv6277574, essv5996187, essv6571220, essv6473472, essv5900972, essv5759249, essv5926190, essv5771644, essv5851534, essv5858162, essv5615811, essv6154954, essv6454547, essv5840977, essv5883731, essv6033744, essv6193268, essv5813573, essv6048655, essv5860916, essv5676681, essv6211701, essv6123074, essv6036806, essv6247670, essv6238797, essv6076538, essv5888316, essv5900623, essv6478291, essv5398254, essv6343310, essv5577223, essv5759894, essv6132184, essv5573195, essv5445341, essv6164165, essv6513069, essv6442299, essv6081084, essv6037981, essv6189230, essv6361904, essv5887792, essv5401950, essv5519727, essv5773046, essv5958398, essv6566774, essv5930926, essv5801045, essv6397833, essv6339911, essv5497634, essv6047386, essv5683213, essv5426670, essv6206513, essv5751769, essv5428622, essv5551529, essv5958274, essv6361992, essv6348029, essv6299793, essv6203502, essv6070088, essv5736871, essv5579177, essv5873679, essv6043589, essv5526067, essv5666545, essv5570267, essv5737153, essv5406920, essv6455637, essv5753310, essv6514786, essv5397654, essv6155479, essv5680632, essv5486316, essv6428963
SamplesHG01060, HG00542, HG00608, NA18621, HG00524, HG01389, HG01374, NA12004, NA18596, HG00449, NA18602, HG00693, HG00337, HG00327, HG00271, HG00127, HG01070, HG00589, HG00251, HG00501, HG01351, HG00330, HG01354, HG01365, HG00590, NA19404, HG00512, HG00139, HG00277, NA19720, HG01067, HG00683, HG01072, HG00232, HG00705, HG01048, HG00326, HG00253, NA11993, HG01353, HG00137, NA12489, NA19657, HG00268, HG01171, HG00328, HG01095, HG00475, HG00320, HG00344, NA18637, HG00275, NA18534, HG00692, HG01390, HG01102, HG00324, HG01073, HG00273, HG00651, HG00479, NA12829, HG00684, HG00321, HG00140, NA12827, HG01334, HG00463, NA18536, HG00246, NA18570, HG01204, NA18632, HG00124, NA18559, HG00353, HG00580, HG00136, HG01375, HG00473, HG00237, HG01108, HG00256, HG00620, HG00672, HG00111, HG00421, NA18636, HG00274, HG00252, NA20502, NA18624, HG00345, NA18612, NA18562
Known GenesNAA60
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665923
Frequency
Sample Size1151
Observed Gain0
Observed Loss95
Observed Complex0
Frequencyn/a


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