A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678873



Internal ID9598292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89325133..89325192hg38UCSC Ensembl
Outerchr15:89324976..89325345hg38UCSC Ensembl
Innerchr15:89868364..89868423hg19UCSC Ensembl
Outerchr15:89868207..89868576hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6183647, essv6042882, essv5800327, essv6284942, essv5931732, essv5679323, essv6524641, essv5614596, essv6569644, essv6093607, essv5501717, essv6081170, essv6352367, essv6365025, essv6242630, essv5601793, essv5611546, essv5571295, essv5807708, essv6078127, essv5855122, essv5979021, essv6088889, essv6005965, essv6272266, essv6168673, essv6236507, essv6385655, essv6008211, essv5878779, essv6362956, essv6277618, essv6409841, essv5867184, essv5958151, essv5544157, essv5417881, essv6593145, essv5600482, essv5679063, essv5505897, essv5834624, essv5562631, essv5403999, essv6271982, essv5603329, essv5667355, essv6029711, essv5588756, essv5555517, essv6209840, essv5947063, essv6579978, essv5965675, essv5696857, essv6275315, essv5554297, essv6321544, essv6287933, essv6482781, essv6337547, essv6582370, essv5456442, essv5817450, essv5525263, essv6210679, essv5600145, essv5684579, essv6432024, essv6559021, essv6027660, essv6409511, essv5493398, essv6548694, essv6504429, essv6045210, essv5740781, essv5694317, essv5647320, essv5565248, essv6192931, essv6370422, essv6039868, essv5948067, essv6511586, essv5429586, essv6496584, essv5469223, essv6178307, essv5439161, essv5888887, essv6563627, essv5886819, essv6330709, essv5632615, essv5752970, essv5588691, essv6144654, essv6536296, essv6494670, essv5818415, essv5653277, essv5703639, essv5941059, essv5640820, essv5402388, essv6342561, essv6304686, essv5832042, essv5818835, essv5526984, essv5905872, essv6431160, essv6405282, essv6168127, essv6359721, essv6335366, essv5599769, essv5965853, essv6392138, essv6133867, essv6406512, essv6484056, essv5960099, essv5599852, essv5478323, essv6403790, essv5669831, essv6414085, essv5967754, essv5881656, essv5909452, essv6115112, essv5976945, essv6317496, essv6211659, essv6146628, essv5839712, essv5843288, essv5867065, essv6420412, essv5642629, essv6452997, essv6036388, essv5923463, essv5759475, essv5473541, essv6114906, essv5538238, essv5652072, essv5437994, essv6258067, essv5440317, essv6197736, essv5904206, essv5611612, essv5463096, essv6524226, essv5571884, essv5730361, essv6408359, essv6492143, essv6316527, essv6565907, essv6452344, essv5813892, essv5635942, essv6331000, essv6194220, essv5405480, essv5421683, essv5603225, essv6087068, essv5638841, essv5964220, essv5809347, essv5589453, essv5516683, essv6336200, essv5826593, essv5398217, essv6058256, essv6156951, essv5841336, essv6132608, essv5505216, essv6541576, essv6194257, essv5985183, essv6242902, essv5534239, essv6041756, essv5659061, essv5447159, essv5953725
SamplesNA20588, HG01060, NA20761, NA11830, HG01173, NA18621, HG00142, NA18947, HG00671, HG00524, HG00187, HG01188, NA11933, HG00257, HG01389, HG01374, HG01066, HG00151, NA18486, NA12751, HG00699, NA18545, NA12004, NA18959, NA18606, NA19190, NA18870, NA18526, HG01051, NA18633, NA20771, NA18602, HG00337, NA07346, HG00138, NA19381, HG01350, NA18550, HG01366, HG00589, HG00501, NA19382, NA20798, NA18595, HG01488, HG00702, HG00689, NA18982, NA18558, NA18547, HG00610, NA11992, NA11918, NA07347, NA20768, HG00369, HG01365, HG00334, NA20513, HG00185, HG00158, NA20541, NA18611, HG00512, HG00281, HG00139, HG01069, HG01080, HG01067, HG00683, HG00335, HG01170, HG00236, HG00325, HG01072, NA19372, NA19385, HG00422, HG00705, NA12889, HG01440, HG00309, HG00182, HG00427, HG00338, HG01048, HG00419, HG00253, NA18638, NA12748, HG00464, HG00108, HG01124, HG00260, NA11831, HG01353, HG00543, HG00313, HG01183, HG01136, NA18951, NA18605, NA19657, HG00443, HG01187, HG01171, HG00282, HG00596, HG00557, HG00328, NA12003, HG00428, HG00657, HG00436, HG00320, HG00584, HG00533, HG00275, HG00619, HG00692, NA18907, HG01047, NA18566, HG01102, HG00324, HG00284, HG01073, NA18573, HG00273, HG00651, HG00250, HG00690, NA12829, HG00331, NA18499, NA18856, HG00613, HG00321, HG00140, NA19099, HG01334, NA18555, HG00704, NA18536, NA18570, NA18593, HG01204, NA18576, NA18546, NA12043, NA18632, HG00124, NA20522, HG00254, HG00336, HG00285, NA18952, NA18543, HG00353, HG00278, NA20520, NA07051, NA12046, HG01375, HG00607, HG00319, HG01108, HG00256, HG00662, HG00418, NA06986, HG00620, HG00707, HG00513, NA20348, HG00329, NA12749, HG00656, NA19093, NA18636, HG00698, HG00280, HG00343, NA20528, NA18552, HG00252, HG00472, HG00345, NA12890, NA18623, NA07000, NA18612, HG01061, HG00581, NA18620
Known GenesPOLG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678873
Frequency
Sample Size1151
Observed Gain0
Observed Loss195
Observed Complex0
Frequencyn/a


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