A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658458



Internal ID9924563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95824120..95824358hg38UCSC Ensembl
chr8:96836348..96836586hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5688466, essv6343048, essv6208501, essv5833846, essv6578212, essv6522002, essv5529396, essv6411808, essv5562470, essv5396086, essv6107474, essv6265595, essv6215570, essv5957677, essv6429501, essv6336715, essv5767311, essv5609627, essv6491173, essv5851484, essv6234445, essv5824520, essv6202133, essv6457981, essv6234488, essv5706082, essv6027970, essv5897681, essv5454216, essv6504582, essv6058418, essv5900978, essv5939226, essv6277874, essv5970447, essv6582776, essv6437670, essv6341243, essv5583813, essv5960279, essv6062017, essv5746767, essv6444592, essv5791762, essv6559178, essv5402936, essv6549673, essv6582069, essv5987227, essv6363568, essv5780646, essv5777705, essv5752583, essv6329452, essv5706842, essv6137180, essv6321855, essv6497686, essv5598563, essv5497795, essv5873695, essv5625768, essv5574014, essv6268155, essv5900472, essv5802801, essv5626706, essv6216925, essv6594912, essv5878682, essv6281431, essv6567651, essv5968573, essv5874924, essv5976573, essv6469944, essv5513890, essv6258874, essv6044830, essv5828808, essv6258421, essv5601662, essv5501378, essv6564120, essv6012125, essv6158066, essv6368775, essv6082684, essv6497019, essv6175829, essv6391347, essv6109098, essv5500785, essv6519612, essv6218585, essv5959083, essv6527841, essv6015404, essv6564695, essv5896731, essv5626824, essv6553552, essv6252916, essv5942780, essv5456643, essv5908413, essv5760661, essv6556901, essv6275666, essv6064547, essv5959576, essv6518102, essv6101813, essv6061568, essv5707717, essv6094151, essv5571352, essv6365539, essv6171600, essv6360138, essv5991030, essv5930781, essv6124474, essv5713754
SamplesHG01060, HG00650, HG00542, HG01521, NA12842, NA19397, NA18621, HG00671, HG00524, HG01052, HG01079, NA11933, HG01374, HG01066, HG00315, HG00699, HG00103, NA19393, NA19377, NA18606, HG01518, HG00449, HG00261, NA18602, HG00693, HG00271, NA19374, NA19396, HG00138, NA18940, HG00251, HG01351, HG00330, HG00346, HG00590, NA18611, HG00281, HG00139, HG01069, HG01080, HG01067, HG00683, HG00232, NA20340, NA19731, HG00422, HG00338, NA18557, HG01048, HG00419, NA19789, HG00464, HG01124, HG01353, HG00543, HG00313, HG01136, NA18613, HG01360, HG00282, NA19403, HG00328, NA19391, HG00475, HG00436, HG00320, HG00584, HG00533, HG00583, NA18948, NA20344, HG00708, HG00692, HG00740, HG01390, HG01073, HG00250, HG00690, HG01383, HG01101, HG00613, HG00525, HG00321, HG00140, HG01334, HG00276, HG00704, HG00246, NA19395, HG01107, NA19436, NA18546, NA19401, NA18632, HG00476, HG00336, HG00285, HG00375, HG00278, HG01357, NA19428, NA19083, HG01108, HG00256, HG00662, HG00418, HG00620, HG00707, HG00672, HG00421, NA19093, HG00698, HG01251, HG01377, HG00472, NA19758, NA18624, NA18623, NA18612, HG01437, HG01061, HG00437, HG00581, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658458
Frequency
Sample Size1151
Observed Gain0
Observed Loss124
Observed Complex0
Frequencyn/a


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