A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672028



Internal ID9938133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42473378..42475078hg38UCSC Ensembl
chrX:42332630..42334330hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5877585, essv5460184, essv5995751, essv6027712, essv6362840, essv5976012, essv5972531, essv6240240, essv5673237, essv6199734, essv5410402, essv6153790, essv6274421, essv6467143, essv5485874, essv5684663, essv6231347, essv5743233, essv5530975, essv6413527, essv6262085, essv6517124, essv5475693, essv5545086, essv6131786, essv5400140, essv6084303, essv5599276, essv6480784, essv5970212, essv5821936, essv5903967, essv6436928, essv6240403, essv6135805, essv5511009, essv6309806, essv5679805, essv6334350, essv6315593, essv6293212, essv6212755, essv6305229, essv6385135, essv5631189, essv5874739, essv6437566, essv6259149, essv5780602, essv5486838, essv5674911, essv6129281, essv6413486, essv5461577, essv6044068, essv5495712, essv5646042, essv6343063, essv5453294, essv5497045, essv5500818, essv5952586, essv6066830, essv6458429, essv5926208, essv6041388, essv6193414, essv5786702, essv6345711, essv6170955, essv5768463, essv5722937, essv6136903, essv5991453, essv5720880, essv5762935, essv6549235, essv5703121, essv5712175, essv6387629, essv6484399, essv5467731, essv6273476, essv6163023, essv6086947, essv5850113, essv6054309, essv5432721, essv5539677, essv6177969, essv5508426, essv5683886, essv6571361, essv5952396, essv6015756, essv6249693, essv5793453, essv5535878, essv6169342, essv6193947, essv5882741, essv5932545, essv6200093, essv5700750, essv6412006, essv6380232, essv6104399, essv5882695, essv5695305, essv5397511, essv5825282, essv5505415, essv6498840, essv6081889, essv6531844, essv5560775, essv5935416, essv6330587, essv5973249, essv5561966, essv6348473, essv6240640, essv6330253, essv6163333, essv5672743, essv5572095, essv5951810, essv6360603, essv6365056, essv6546784, essv6470501, essv6061522, essv6221618, essv5644068, essv5610307, essv5746890, essv6168382, essv6138403, essv5862638, essv5984192, essv5745302, essv6300797, essv6297356, essv5575158, essv5727271, essv5822260
SamplesNA19394, NA18502, NA19701, NA19700, NA18924, NA19909, NA18861, NA18508, NA19399, HG01052, NA19332, NA12414, NA19704, NA19350, NA18486, NA20294, NA19355, NA19819, NA18504, NA19377, NA20346, NA18870, NA20356, NA19107, NA19374, NA19396, NA19171, NA19379, NA19005, NA18519, NA19319, HG01167, NA19198, NA19916, NA19131, NA18960, NA18916, NA19197, NA07347, HG01083, NA19138, NA18498, NA20336, NA19384, NA19404, NA19383, NA18868, NA19917, NA19719, NA19137, NA19371, NA19238, NA11994, NA19235, NA19385, NA19172, NA19471, NA19189, NA18520, NA19239, NA20127, NA18908, NA19985, NA18867, NA19921, NA19908, NA19247, NA19437, HG01171, NA19403, NA19462, NA19347, NA18933, NA19327, NA19236, NA18516, NA19982, NA18871, NA20344, NA18907, HG01102, HG01094, NA19461, NA19114, NA20299, NA19449, NA18499, NA18856, NA19453, NA18912, NA19099, NA19338, NA19257, NA19452, NA19225, NA18523, NA19395, NA19625, NA18858, NA19436, NA19440, NA19390, NA18909, NA19108, NA19256, NA19147, NA20276, NA19712, NA19473, HG00734, NA19435, NA19444, NA19240, NA19835, NA19334, NA19439, NA19324, NA19311, HG01108, NA20281, NA20341, NA19376, NA19398, NA18501, NA19472, NA19223, NA20334, NA19713, NA19474, HG01055, NA19093, NA19102, NA18873, NA19116, NA19711, NA19213, NA19900, NA19129, NA18488, NA19758, NA20322, NA19463, NA18511, NA19346, NA18487, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672028
Frequency
Sample Size1151
Observed Gain0
Observed Loss146
Observed Complex0
Frequencyn/a


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