A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661835



Internal ID9927940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28373337..28375843hg38UCSC Ensembl
Outerchr10:28372816..28376363hg38UCSC Ensembl
Innerchr10:28662266..28664772hg19UCSC Ensembl
Outerchr10:28661745..28665292hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383548
hg193548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6326727, essv6310948, essv6289744, essv5783716, essv5428260, essv6238192, essv5937743, essv5553459, essv5939530, essv5555490, essv5467360, essv5455973, essv5966452, essv6014924, essv6304750, essv5675433, essv6019657, essv6114644, essv6028362, essv6294539, essv6467172, essv6200429, essv5540276, essv5958527, essv6461381, essv5616592, essv6357298, essv6219234, essv6066182, essv5988398, essv5600066, essv6440820, essv5592196, essv6298082, essv5965691, essv5793160, essv5495400, essv6150317, essv5904420, essv5474028, essv6462744, essv6082844, essv6562590, essv6526717, essv5838912, essv5438395, essv6428638, essv5892378, essv5890672, essv6518249, essv6443372, essv6333339, essv5941362, essv5541791, essv6515331, essv5563643, essv6473498, essv5687568, essv5485950, essv6543353, essv5824172, essv5647445, essv6283845, essv6181068, essv5431810, essv5489367, essv6527574, essv6416647, essv6573991, essv6007284, essv6541835, essv5716377, essv6284145, essv5790026, essv5740405, essv6369105, essv6332218, essv5714445, essv5506160, essv6546217, essv5530229, essv6349233, essv6097776, essv5496270, essv5707357, essv5505860, essv6400770, essv6505933, essv5422296, essv6264953
SamplesHG00650, HG00542, HG00442, HG00536, HG00608, HG00671, HG00361, HG00524, HG00187, HG00315, HG00693, NA18627, HG00327, NA18550, HG00272, HG00501, NA18595, HG00689, NA18619, NA18558, HG00330, HG00634, HG00610, HG00185, HG00537, HG00512, NA18560, HG00534, HG00705, HG00182, HG00427, HG00323, HG00530, HG00419, HG00464, HG00543, HG00313, HG00188, HG00560, NA18613, HG00268, HG00557, HG00328, HG00653, HG00436, HG00556, HG00533, HG00583, HG00500, HG00275, NA18534, HG00619, HG00708, HG00692, NA18537, NA18566, NA18626, HG00690, HG00531, HG00684, HG00525, HG00276, NA18536, NA18593, NA18541, HG00476, NA18542, HG00285, NA18559, HG00353, HG00375, HG00473, HG00662, HG00418, HG00620, HG00707, HG00614, HG00513, HG00478, NA18631, HG00421, HG00698, HG00343, HG00472, HG00628, HG00345, NA18612, NA18549, NA18562, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661835
Frequency
Sample Size1151
Observed Gain0
Observed Loss90
Observed Complex0
Frequencyn/a


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