A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671009



Internal ID9937114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8692692..8692873hg38UCSC Ensembl
chr17:8596010..8596191hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv533e199
Supporting Variantsessv5517435, essv5491268, essv5686917, essv5586092, essv6405093, essv6435273, essv5560833, essv6385821, essv5688159, essv6230517, essv6334608, essv6340326, essv6368007, essv6038403, essv6313457, essv5709356, essv5924394, essv6229444, essv5829355, essv5834274, essv6197647, essv5758560, essv5491600, essv6009215, essv5880828, essv6047288, essv6097150, essv5629994, essv5482902, essv6048035, essv5980391, essv6548002, essv6049262, essv5766413, essv6049936, essv6036610, essv5839249, essv5781833, essv5684186, essv5801213, essv5436356, essv5819522, essv5694081, essv6591242, essv5864491, essv6174699, essv6022927, essv5877236, essv5588253, essv5404975, essv6400926, essv6469304, essv6092783, essv6051718, essv5515630, essv5415427, essv5750995, essv5425558, essv6450501, essv6534534, essv5662948, essv5426826, essv6092204, essv6476809, essv6410646, essv5880128, essv5829670, essv6358855, essv6284562, essv5924102, essv5926866, essv5947236, essv6325966, essv6196932, essv6399472, essv6277670, essv6462021, essv6471924, essv6258957, essv5463957, essv6552085, essv5482705, essv6062296, essv5466433, essv6155671, essv5910186, essv5819938, essv5714276, essv5548571, essv6218662, essv6229745, essv5745864, essv5537885, essv6002262, essv6076303
SamplesNA19394, HG00542, HG00442, NA19397, NA19664, HG00671, NA19399, NA18486, NA19819, NA18596, HG00177, HG01051, NA18633, NA19076, HG01350, NA19379, NA18940, HG01366, NA18595, HG01488, HG00346, NA18498, HG00537, HG00590, NA19720, HG01067, NA19383, HG00683, HG00232, NA20340, NA19372, NA19371, HG00534, HG00422, HG01440, HG00427, NA18557, HG01133, HG00323, HG00419, HG00464, HG00313, NA18544, NA18613, NA19657, HG01171, HG00557, HG00428, HG00653, HG00701, NA19391, HG00475, NA19663, HG00556, HG00583, NA18637, NA18534, NA18548, HG01390, NA18566, HG00273, HG00531, NA18856, HG01383, HG01101, HG00613, HG00321, HG00704, HG00246, NA18634, HG01107, HG01204, HG01148, NA18961, NA18559, NA19434, HG00375, HG00136, HG00473, NA19428, HG00256, HG00662, HG00418, HG00614, HG00329, HG00656, NA20334, HG01055, NA19770, HG00698, HG00280, HG00372, HG00437, NA18562, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671009
Frequency
Sample Size1151
Observed Gain0
Observed Loss95
Observed Complex0
Frequencyn/a


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