A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667494



Internal ID9933599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99373554..99373596hg38UCSC Ensembl
Outerchr7:99373397..99373749hg38UCSC Ensembl
Innerchr7:98971177..98971219hg19UCSC Ensembl
Outerchr7:98971020..98971372hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6440996, essv5414027, essv6585366, essv5958304, essv5834848, essv5695129, essv6057698, essv6474524, essv5887451, essv5874332, essv6583368, essv6511836, essv5906205, essv6047253, essv6561147, essv5440217, essv5612865, essv5724269, essv5896615, essv5583398, essv5753492, essv6174753, essv6029788, essv6254415, essv6591731, essv5946770, essv6587834, essv5937191, essv6094781, essv5716258, essv5912071, essv5740555, essv5520060, essv6058785, essv5724727, essv6572313, essv6175867, essv6045024, essv6290490, essv5789003, essv5719664, essv6015292, essv5545010, essv6123559, essv6529201, essv6504475, essv6414313, essv5586922, essv6179620, essv5416426, essv6411817, essv6397949, essv5436495, essv5537844, essv6053331, essv6349359, essv5910986, essv5406818, essv5906868, essv6145516, essv5900544, essv6573103, essv6564495, essv6455770, essv5624015, essv5675883, essv5595763, essv5617338, essv6244848, essv5808486, essv6117877, essv6459159, essv5829105, essv6131948, essv6566495, essv5781175, essv6323402, essv6399324, essv6155409, essv6317065, essv6476311, essv6299815, essv6104649, essv6029380, essv5883066, essv6256130, essv5570671, essv6173088, essv5422587, essv5909569, essv5856304, essv5647971, essv6480847, essv6124302, essv6541986, essv5523840, essv6491011, essv5663316, essv5970308, essv6278605, essv5456916, essv6488207, essv6441363, essv6496616, essv6255971, essv6572329, essv6557794, essv6250261, essv5958314, essv6314780, essv5870381, essv6193043, essv5736037, essv6097664, essv5838650, essv6153678, essv6039605, essv5841251, essv5758773, essv6388268, essv6593546, essv6190866, essv5954270, essv5594833, essv5543954, essv5663359
SamplesNA19394, HG01060, NA19701, NA19700, HG01356, NA20543, NA19703, NA19397, NA19466, NA18592, NA19399, NA20783, HG01079, HG01188, NA18917, NA18486, NA20294, NA19355, NA19443, NA19190, HG01051, NA19920, NA18510, NA19374, HG00641, NA19396, HG00138, NA19381, NA19373, HG01350, NA19379, NA18519, NA19319, NA19728, NA20317, NA19916, NA20540, NA19457, HG01083, NA19782, NA20291, NA19130, HG00281, NA19383, NA20775, NA18868, NA19719, HG00232, NA19372, NA19371, NA19471, NA19317, NA19901, HG01048, NA19445, NA20127, HG00137, HG00188, NA19908, HG00183, HG01384, NA19403, NA20505, NA19462, NA18933, HG00732, NA20521, NA19391, NA19455, NA18516, NA19982, NA20126, NA18910, NA18871, HG01390, HG00324, HG00284, NA19461, NA19449, HG00373, NA20581, NA18856, NA19750, NA18853, HG00152, NA19625, NA19401, NA19375, NA19390, NA19834, NA18517, NA19434, NA12775, HG00353, NA19473, HG00136, NA19331, HG01174, NA19835, NA19334, NA19679, NA19470, NA19428, NA19324, NA19311, NA19467, NA20281, NA19360, HG01342, NA06986, NA19376, NA19248, NA19472, NA19223, NA19713, NA19093, NA18873, NA19116, NA19213, NA19900, NA18488, HG01082, NA19312, NA19463, NA19346, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667494
Frequency
Sample Size1151
Observed Gain0
Observed Loss126
Observed Complex0
Frequencyn/a


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