A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660901



Internal ID9580320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60334561..60336585hg38UCSC Ensembl
chr17:58411922..58413946hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv559e199
Supporting Variantsessv5928588, essv5709345, essv5403538, essv5620591, essv6302877, essv5903531, essv5731464, essv6583778, essv5447871, essv5489474, essv6021852, essv5657552, essv6542425, essv5850042, essv5664068, essv6537964, essv5510351, essv5454064, essv6372031, essv6155227, essv5848505, essv5843174, essv6185274, essv5985200, essv5616644, essv5953275, essv5634420, essv6367705, essv6183733, essv5437851, essv6324861, essv6496986, essv6257406, essv6412797, essv6568608, essv6249069, essv5466030, essv5941014, essv6052844, essv5896836, essv6512186, essv5567593, essv6070237, essv5905720, essv5481898, essv5466549, essv6144531, essv5734847, essv6098672, essv5409738, essv6348208, essv6520576, essv5853048, essv5557986, essv5997411, essv6321159, essv6222645, essv5766948, essv5568551, essv5436388, essv5761534, essv6542278, essv5505450, essv6439738, essv5540314, essv6386762, essv6193603, essv6034976, essv6297223, essv5453813, essv6526315, essv5658042, essv5547426, essv6138085, essv6218423, essv6289872, essv6182283, essv6231953, essv6236046, essv5947400, essv6087367, essv6584913, essv6157462, essv5943024, essv6318722, essv6517666, essv6559435, essv6143747, essv6188911, essv5647220, essv6578440, essv6163273, essv5751038, essv6253715, essv5873069, essv6179376, essv5526757, essv6436637, essv5527484, essv6387074, essv5473160, essv6415862, essv6366672, essv6201097, essv5664330, essv6074096, essv5715724, essv6078101, essv6430157, essv6477413, essv5835462, essv6356855, essv6008547, essv5438188, essv5405095, essv5741054
SamplesHG01441, NA19397, NA18924, HG01462, NA19909, NA20508, NA19466, NA19332, NA19704, HG00315, NA19359, HG01465, NA19355, NA19819, NA19057, NA19684, HG00737, NA20346, NA20507, HG01051, HG01140, HG00337, NA19107, NA19374, HG00641, NA19396, NA19381, NA19373, HG01488, NA18923, NA19457, HG01083, HG00247, HG00369, HG01365, NA19681, NA20291, NA19130, HG01134, NA18874, NA20340, NA19235, NA19471, NA19317, HG01198, HG00637, HG01048, NA19445, NA18867, HG00530, NA19921, NA19247, HG00176, NA19462, NA19347, NA20809, HG01095, NA19455, HG00584, HG01149, HG00692, HG01390, HG01047, NA19461, NA19449, NA19655, NA19453, NA18963, NA18523, NA19469, NA19625, NA19436, NA18576, NA19401, NA19375, NA18632, NA19652, NA19440, NA19390, HG00265, NA19834, NA19434, NA19473, NA19072, NA19435, NA18941, HG01375, NA19835, NA19439, NA19470, NA19311, HG01108, NA19360, NA20341, NA19818, NA19376, NA19398, NA19472, NA19223, NA19713, NA19213, NA19900, NA19430, HG01082, NA19316, HG00628, NA20322, NA18624, NA19463, HG01097, NA18612, NA19429, NA18487, HG00553, NA19431, NA18620
Known GenesUSP32
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660901
Frequency
Sample Size1151
Observed Gain0
Observed Loss116
Observed Complex0
Frequencyn/a


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