A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1406e199



Internal ID22759179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151173673..151179820hg38UCSC Ensembl
chrX:150342145..150348292hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386148
hg196148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666356, esv2659185
SamplesNA20588, NA19394, HG00650, HG00542, HG00442, HG01173, HG00608, NA20766, HG00671, HG00559, NA20783, NA20514, HG01066, NA20816, NA20752, NA20512, NA19350, NA19359, HG00737, NA19443, HG01051, NA20806, NA20814, NA19446, HG00641, NA19373, HG00589, NA19319, NA20798, NA20589, HG01167, NA20774, NA19457, NA19384, HG00537, HG00512, NA20759, NA20539, HG01069, NA20518, NA20775, NA20812, NA19372, HG01048, NA20757, NA20515, NA20755, HG00731, HG00443, HG00732, NA20521, NA20810, NA19455, HG00556, HG00583, NA20519, HG00692, HG00740, HG01047, NA20525, HG01102, NA19461, HG00651, HG00690, HG00404, HG00531, NA20581, HG00684, NA19453, HG01101, NA19452, HG00704, HG00463, NA19469, NA19318, HG01107, HG01075, NA19375, HG00611, NA19440, HG00625, NA19434, NA20815, HG00580, HG00734, NA19444, NA19331, NA20520, NA20790, NA20530, NA20527, HG00473, NA20792, NA20778, NA19470, NA19428, NA19324, NA19311, NA20544, NA19360, HG00662, HG00418, HG00620, NA19328, HG00614, HG00478, NA19468, NA19474, NA20510, NA20786, NA20758, HG00595, NA19430, NA19312, HG00628, NA19463, NA20754, NA19429, NA19346, HG00553, NA19431, NA20772, HG00593, HG00626, HG00403, HG01060, HG00592, NA20543, HG00536, NA19397, NA19466, HG00524, HG01052, NA19332, HG01079, HG01188, NA20532, HG00640, HG00699, NA19393, NA20805, HG00566, NA20507, NA20537, NA19374, NA20796, NA19382, NA19448, HG00702, HG00689, HG00448, NA20586, NA20769, HG00634, HG00736, HG00610, NA19313, NA20513, HG00590, NA19383, HG00683, NA20819, HG01170, HG01072, NA19371, NA19385, NA19317, HG01176, HG00427, NA20811, HG00637, NA19456, NA19445, NA20533, HG00530, NA19451, NA20818, HG00543, HG00560, HG00629, NA19437, HG01187, NA20787, HG00596, NA20524, HG00428, NA19462, NA19347, NA20809, HG00653, HG00577, HG00701, NA20536, NA19327, HG00475, HG00436, HG00533, HG00500, NA20506, NA20770, HG00619, HG00635, NA19449, HG01197, NA20538, HG01182, HG00613, NA20542, NA20534, HG01204, NA20765, HG00476, NA20801, HG01190, NA19321, HG00565, NA19473, NA19435, HG00638, NA19380, NA20785, NA19334, HG00607, NA19439, NA20516, HG01108, NA20803, NA19376, HG00707, HG00672, HG00578, NA19438, HG00421, HG00656, HG00698, NA20528, HG00472, HG01082, HG01097, HG01061, HG00437, NA20509
Known GenesGPR50
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1406e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss242
Observed Complex0
Frequencyn/a


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