A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625335



Internal ID7012169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9482211..9487582hg38UCSC Ensembl
Innerchr11:9482211..9487582hg38UCSC Ensembl
Outerchr11:9481887..9487924hg38UCSC Ensembl
chr11:9503758..9509129hg19UCSC Ensembl
Innerchr11:9503758..9509129hg19UCSC Ensembl
Outerchr11:9503434..9509471hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385372
hg195372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14023766, essv14023749, essv14023769, essv14023688, essv14023768, essv14023729, essv14023733, essv14023709, essv14023705, essv14023731, essv14023760, essv14023763, essv14023734, essv14023703, essv14023758, essv14023687, essv14023740, essv14023708, essv14023745, essv14023764, essv14023718, essv14023698, essv14023726, essv14023770, essv14023725, essv14023720, essv14023706, essv14023695, essv14023737, essv14023722, essv14023716, essv14023750, essv14023712, essv14023692, essv14023767, essv14023724, essv14023753, essv14023697, essv14023730, essv14023739, essv14023765, essv14023711, essv14023738, essv14023735, essv14023715, essv14023746, essv14023759, essv14023747, essv14023751, essv14023732, essv14023682, essv14023693, essv14023771, essv14023774, essv14023701, essv14023710, essv14023736, essv14023719, essv14023699, essv14023690, essv14023700, essv14023757, essv14023727, essv14023773, essv14023704, essv14023752, essv14023755, essv14023684, essv14023728, essv14023762, essv14023741, essv14023717, essv14023689, essv14023742, essv14023686, essv14023721, essv14023744, essv14023754, essv14023702, essv14023756, essv14023743, essv14023748, essv14023685, essv14023723, essv14023683, essv14023694, essv14023714, essv14023696, essv14023691, essv14023713, essv14023772, essv14023761, essv14023707, essv14023681
SamplesNA19394, NA18502, HG02890, HG02944, HG02628, HG02583, HG03163, HG01052, NA18507, HG02852, HG02891, HG02870, HG03280, NA19355, HG03515, HG02589, NA19190, NA19920, HG02895, HG03464, NA19379, HG02621, NA19448, NA19307, HG03091, HG02595, HG02645, NA19197, HG03578, HG03224, HG02703, HG03556, NA18874, HG02573, NA19917, NA19238, NA19024, HG02885, NA19172, NA19471, NA18908, HG03048, HG02977, NA19908, NA19984, HG02449, HG02253, HG01882, HG03457, NA19982, NA18910, HG02470, HG03124, HG01092, HG03301, NA18879, HG02309, NA19320, HG03024, NA19099, HG02979, NA18523, HG02635, HG02594, HG02484, HG03064, NA19256, HG03437, NA19434, NA19037, HG03127, NA19439, HG02941, NA19310, HG03473, HG02464, HG02580, HG02814, HG03103, NA19351, HG02646, HG02053, HG03060, HG02462, HG01914, HG02947, HG02465, NA19463, HG01886, HG02808, HG03118, HG00553, NA19153, HG03265
Known GenesZNF143
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625335
Frequency
Sample Size2504
Observed Gain0
Observed Loss94
Observed Complex0
Frequencyn/a


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