A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645595



Internal ID7032344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25715537..25727136hg38UCSC Ensembl
chr20:25696173..25707772hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16166642, essv16166580, essv16166534, essv16166563, essv16166634, essv16166599, essv16166641, essv16166592, essv16166594, essv16166609, essv16166540, essv16166616, essv16166582, essv16166547, essv16166611, essv16166584, essv16166637, essv16166635, essv16166631, essv16166572, essv16166569, essv16166560, essv16166610, essv16166643, essv16166646, essv16166537, essv16166644, essv16166579, essv16166624, essv16166651, essv16166625, essv16166554, essv16166617, essv16166557, essv16166544, essv16166597, essv16166601, essv16166591, essv16166583, essv16166533, essv16166606, essv16166588, essv16166612, essv16166558, essv16166542, essv16166536, essv16166535, essv16166581, essv16166618, essv16166546, essv16166564, essv16166640, essv16166549, essv16166577, essv16166541, essv16166545, essv16166556, essv16166604, essv16166627, essv16166614, essv16166574, essv16166602, essv16166578, essv16166573, essv16166548, essv16166639, essv16166603, essv16166623, essv16166615, essv16166566, essv16166543, essv16166608, essv16166555, essv16166605, essv16166649, essv16166633, essv16166596, essv16166648, essv16166562, essv16166567, essv16166539, essv16166570, essv16166613, essv16166620, essv16166576, essv16166600, essv16166575, essv16166626, essv16166622, essv16166586, essv16166551, essv16166553, essv16166619, essv16166552, essv16166593, essv16166550, essv16166630, essv16166568, essv16166561, essv16166587, essv16166538, essv16166607, essv16166571, essv16166585, essv16166559, essv16166532, essv16166638, essv16166565, essv16166647, essv16166636, essv16166628, essv16166595, essv16166632, essv16166650, essv16166590, essv16166589, essv16166645, essv16166598, essv16166629, essv16166621
SamplesNA18998, HG02072, HG00671, NA19066, HG01860, HG01815, HG02122, HG02275, NA20813, HG00244, HG01806, HG00181, NA12751, NA19355, HG01486, HG00452, NA19057, HG02382, NA19669, HG02023, NA18969, HG03009, HG01500, NA19068, HG01506, HG00356, NA20796, HG01366, HG00272, HG01853, HG02140, HG00599, HG01945, NA18942, NA19062, HG00346, HG01848, HG01982, HG01668, HG01372, NA19079, HG03594, HG01859, NA20759, HG02493, NA18970, HG00335, HG02224, HG01757, HG01495, HG01527, NA18966, HG00309, NA18985, HG01771, HG02409, HG01851, HG00675, HG00543, HG00349, HG00133, HG00290, NA20854, NA20892, NA12489, HG01867, HG00266, NA19091, NA19082, NA19006, NA20810, HG03928, HG02076, HG02084, NA18939, HG01845, HG01498, NA20767, HG01607, HG01630, NA21116, HG01047, HG01414, HG00651, HG00331, NA12249, HG01182, NA19059, HG00376, NA18646, HG01811, HG00336, HG00285, NA18543, HG04026, HG01253, NA19435, NA20520, HG01623, HG00308, NA20792, NA18643, HG00662, HG02398, HG00707, HG02373, HG01028, NA19726, NA19080, HG02028, HG01920, NA18968, NA18624, HG01869, NA19063, NA12154, HG01805, NA20754, HG01437, HG00593
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645595
Frequency
Sample Size2504
Observed Gain120
Observed Loss0
Observed Complex0
Frequencyn/a


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