A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673786



Internal ID9593205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28534679..28535528hg38UCSC Ensembl
chr7:28574297..28575146hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1189e199
Supporting Variantsessv5857998, essv6054007, essv6371546, essv6254131, essv5991455, essv6306825, essv5539869, essv6010458, essv5725414, essv5411647, essv6144123, essv5615516, essv6403905, essv5768568, essv5491251, essv6271050, essv6430344, essv6547937, essv5658683, essv6383374, essv6565237, essv6210467, essv5561362, essv6317386, essv6395083, essv6210236, essv6397357, essv6114868, essv6217758, essv6231476, essv5566946, essv6306574, essv5975963, essv5598266, essv6120069, essv6054603, essv5630965, essv5826612, essv5905118, essv6361310, essv5493413, essv5663932, essv5421030, essv5637827, essv5501901, essv5779923, essv6582280, essv5676313, essv6307822, essv6518940, essv6092307, essv6002552, essv6304717, essv6128948, essv5395573, essv5746449, essv5822759, essv6194311, essv5999822, essv6295180, essv6371873, essv5497386, essv6477844, essv5596963, essv5704224, essv6578503, essv6209566, essv6396329, essv6536775, essv6329372, essv5401166, essv6218039, essv6330648, essv6359657, essv6447703, essv6456279, essv6059926, essv5799585, essv5762356, essv5918735, essv5961354, essv6019034, essv5752076, essv5753709, essv5955128, essv6245468, essv5404492, essv5425781, essv5505575, essv5491071, essv5612386, essv6512136, essv6272578, essv6441976, essv6299728, essv5911126, essv6045560, essv5558740, essv5424168, essv6057591, essv5935824, essv6521946, essv6439254, essv6571543, essv5536816, essv5847021, essv6164916, essv5876153, essv5780624, essv6510212, essv5605585, essv5634004, essv5429609, essv5904242, essv6456132, essv5492240, essv6181464, essv6297744, essv5766788, essv5892190, essv5964313, essv6375867, essv5401390, essv6112633, essv5454952, essv6238064, essv5962572, essv5918797, essv6205131, essv5875556, essv5869291, essv5712880, essv5999067, essv6392431, essv5629523, essv6055015, essv6229642, essv6055413, essv5455921, essv6398363, essv5509840, essv6541645, essv6229674, essv5575867, essv6303998, essv6503689, essv6224581, essv5401178, essv5657823, essv6103782, essv6122661, essv6456472, essv6479328, essv6262867, essv5894058, essv6433785, essv5509628, essv6398292, essv6167803, essv5421681, essv6309203
SamplesHG01441, NA19012, HG01515, NA12154, HG00152, HG00734, HG00252, HG00536, HG01440, NA18616, HG01072, NA19819, HG01173, HG01083, NA20510, HG00464, NA20544, HG00736, NA19003, HG00261, NA19223, NA06989, NA20299, HG00463, HG01051, HG01365, HG00117, NA19453, HG01082, NA20529, NA19449, HG00173, HG00326, HG00148, NA20786, HG00139, HG00190, NA19379, HG01167, NA20805, HG00111, HG00334, HG01204, NA07051, HG00651, NA19004, HG00335, NA19701, NA12341, NA19472, NA19761, HG01171, HG00247, HG00554, HG00342, HG01107, NA19062, HG00158, HG01148, NA19067, HG00346, HG01140, HG01375, NA19390, NA18566, HG00337, HG01378, NA19068, NA19660, NA18576, HG00259, NA18623, NA19471, NA19900, HG01048, HG01061, NA18617, HG00372, NA18636, NA19396, NA19397, NA07048, NA19440, HG00258, NA11843, HG01136, HG00243, NA19679, HG00276, HG00284, NA20341, NA19676, HG00159, HG00267, NA19380, NA12046, HG00108, NA12716, HG01465, HG00268, HG01066, NA19373, HG00325, NA20826, NA06986, NA19664, NA19901, HG01069, HG00249, NA18487, HG00116, NA19347, HG00103, NA20582, HG00329, HG00512, HG00534, NA19707, HG00246, HG00525, NA19074, NA19462, HG01149, NA19777, HG00120, NA19235, NA10851, HG01137, NA19376, NA12272, HG00443, NA18909, NA19078, NA18867, NA12413, NA19116, HG00262, NA18631, NA19431, NA18560, HG01112, NA18602, HG01390, NA11830, HG00123, NA19655, HG01366, HG00367, HG00566, NA11829, HG00275, HG00183, HG01522, NA19350, HG01377, HG00143, HG00336, HG00271, NA19779, HG00136, HG01067
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673786
Frequency
Sample Size1151
Observed Gain0
Observed Loss161
Observed Complex0
Frequencyn/a


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