A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622226



Internal ID7009085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5207933..5209032hg38UCSC Ensembl
Innerchr10:5207934..5209032hg38UCSC Ensembl
Outerchr10:5207933..5209033hg38UCSC Ensembl
chr10:5249896..5250995hg19UCSC Ensembl
Innerchr10:5249897..5250995hg19UCSC Ensembl
Outerchr10:5249896..5250996hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13685526, essv13685456, essv13685507, essv13685473, essv13685481, essv13685435, essv13685514, essv13685505, essv13685440, essv13685448, essv13685518, essv13685534, essv13685463, essv13685465, essv13685501, essv13685509, essv13685466, essv13685497, essv13685442, essv13685530, essv13685482, essv13685479, essv13685533, essv13685451, essv13685536, essv13685433, essv13685506, essv13685513, essv13685493, essv13685520, essv13685486, essv13685524, essv13685543, essv13685503, essv13685445, essv13685495, essv13685519, essv13685498, essv13685477, essv13685487, essv13685437, essv13685542, essv13685508, essv13685546, essv13685521, essv13685471, essv13685446, essv13685462, essv13685478, essv13685490, essv13685441, essv13685474, essv13685476, essv13685540, essv13685539, essv13685512, essv13685454, essv13685510, essv13685480, essv13685525, essv13685499, essv13685516, essv13685472, essv13685453, essv13685434, essv13685483, essv13685458, essv13685485, essv13685439, essv13685544, essv13685529, essv13685528, essv13685449, essv13685467, essv13685535, essv13685527, essv13685500, essv13685504, essv13685531, essv13685460, essv13685443, essv13685491, essv13685452, essv13685545, essv13685469, essv13685464, essv13685447, essv13685488, essv13685537, essv13685511, essv13685522, essv13685470, essv13685538, essv13685492, essv13685436, essv13685541, essv13685475, essv13685484, essv13685494, essv13685450, essv13685438, essv13685468, essv13685515, essv13685457, essv13685532, essv13685523, essv13685489, essv13685502, essv13685517, essv13685459, essv13685461, essv13685455, essv13685444, essv13685496
SamplesNA19701, HG02339, HG02944, HG02481, HG01462, NA19204, NA18508, HG03175, HG02419, NA18917, NA20321, NA19092, HG02323, HG03298, NA20294, NA20298, HG03100, HG02888, HG02536, NA19190, NA19098, NA19374, NA19319, NA19201, HG03499, NA20320, NA18923, HG02595, HG03370, NA19131, NA18916, HG03578, HG03224, NA19384, HG02561, HG03556, HG03212, NA19471, NA19026, NA20412, NA20342, NA18908, HG02943, HG02977, HG02439, HG03160, HG03132, HG03363, HG03547, HG01879, HG02887, HG02307, HG02470, HG02537, HG01889, HG03124, NA19118, HG03446, HG02881, HG03451, HG02979, NA19452, HG02585, HG01890, NA19225, HG02332, NA19160, NA19395, NA19035, NA19401, HG02613, NA19309, HG02807, NA18909, HG03240, NA19321, HG03461, NA19147, NA19434, NA19019, NA19454, HG02983, NA19037, NA19439, NA19310, HG03304, HG02464, HG02317, HG03108, HG02558, HG03103, NA19818, HG03432, HG01912, NA19472, NA19223, HG02938, HG02053, HG01254, HG03063, NA19213, HG03538, HG03401, HG01914, NA19030, NA19129, NA18488, NA19312, HG02465, HG02284, HG03303, HG03129, HG03166, HG03196
Known GenesAKR1C4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622226
Frequency
Sample Size2504
Observed Gain0
Observed Loss114
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer