A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677412



Internal ID9943517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27767976..27768269hg38UCSC Ensembl
chr11:27789523..27789816hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5846285, essv6518741, essv5670982, essv5740324, essv6340498, essv5713984, essv5721379, essv6407648, essv5522928, essv5913919, essv6027030, essv6084280, essv6513709, essv6512943, essv5832484, essv5678969, essv6041349, essv5980609, essv5521917, essv5486831, essv5940975, essv6535865, essv5736526, essv5855867, essv6406687, essv6504406, essv6012770, essv6267769, essv6544933, essv6049187, essv6029856, essv6180567, essv5600167, essv5720061, essv6328027, essv5734739, essv6178216, essv5853463, essv5778157, essv6051403, essv5633655, essv6237158, essv6033414, essv5988505, essv5559373, essv6441808, essv6273937, essv5711085, essv6102275, essv5804456, essv6536137, essv6576467, essv5710593, essv5838324, essv6112106, essv6206826, essv6457582, essv5443296, essv6298645, essv5785811, essv6111799, essv5472193, essv5928570, essv5913125, essv5832518, essv5497232, essv6019780, essv5831390, essv6239131, essv6111783, essv5888788, essv5931941, essv5682591, essv5456964, essv5979300, essv5723224, essv5437307, essv6072317, essv5541610, essv6517243, essv5829984, essv6392106, essv6074288, essv6289664, essv5970068, essv6381491, essv5876756, essv5606908, essv6189168, essv5857408, essv6037702, essv5839917, essv5518794, essv6105924, essv6034738, essv5781858, essv5827802, essv6127281, essv5436115, essv6040570, essv6330818, essv5707987, essv5776319, essv5854942, essv5627157, essv5718072, essv5433709, essv5768099, essv6437382, essv6094278, essv5663040, essv5817304, essv5401581, essv6343535, essv6029217, essv6544410, essv5635952, essv5972501, essv5599576, essv6596206, essv5976446, essv5805806, essv5581099, essv5623060
SamplesNA19394, HG00650, HG00442, NA19909, NA18621, HG00142, HG00361, NA19399, NA19914, NA19332, NA18565, NA18599, HG01066, NA19350, NA07357, HG01140, HG00663, NA19374, NA19076, NA18940, NA18550, HG00589, HG00501, HG00702, NA18982, HG00610, HG00346, NA19088, NA18571, HG01365, HG00185, HG00537, HG00683, HG01170, NA19372, NA18560, NA19471, HG00705, NA19087, NA19002, HG00427, NA18990, NA18520, NA18557, NA18985, NA18973, HG00530, HG00419, NA18539, NA18638, HG00464, HG00108, HG00313, NA18951, NA18613, HG00629, HG00443, HG00183, NA19707, NA19056, HG01384, HG00428, NA18956, HG00436, HG00320, HG00583, NA19081, HG00275, HG00692, NA18537, HG00324, HG00651, NA19084, HG00690, HG00404, HG00531, HG00479, HG00331, HG01383, HG01101, NA18553, NA19009, HG00276, HG00704, NA18570, NA18593, NA19401, NA19375, NA18632, NA18542, NA19440, NA12716, HG01190, HG00336, NA18952, NA18543, HG00625, NA19473, NA12272, NA19010, NA07037, HG00662, HG00418, NA18610, HG00269, HG00614, HG00111, HG00578, HG00478, HG00312, NA18987, HG00656, NA18636, NA18609, NA19770, NA18552, NA18989, NA19004, HG00628, NA20322, NA18511, NA18522, NA18622, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677412
Frequency
Sample Size1151
Observed Gain0
Observed Loss124
Observed Complex0
Frequencyn/a


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