A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596054



Internal ID16036777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166083189..166083657hg38UCSC Ensembl
Innerchr4:167004341..167004809hg19UCSC Ensembl
Innerchr4:167223791..167224259hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38469
hg19469
hg18469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9371n54
Supporting Variantsnssv1012569, nssv1012669, nssv1012610, nssv1012675, nssv1012663, nssv1012648, nssv1012666, nssv1012699, nssv1012642, nssv1012712, nssv1012606, nssv1012581, nssv1012584, nssv1012709, nssv1012680, nssv1012698, nssv1012634, nssv1012691, nssv1012687, nssv1012617, nssv1012672, nssv1012612, nssv1012704, nssv1012613, nssv1012668, nssv1012589, nssv1012619, nssv1012575, nssv1012635, nssv1012579, nssv1012640, nssv1012614, nssv1012694, nssv1012627, nssv1012713, nssv1012674, nssv1012563, nssv1012653, nssv1012629, nssv1012682, nssv1012624, nssv1012688, nssv1012643, nssv1012637, nssv1012693, nssv1012676, nssv1012633, nssv1012692, nssv1012703, nssv1012644, nssv1012705, nssv1012662, nssv1012659, nssv1012632, nssv1012616, nssv1012560, nssv1012583, nssv1012641, nssv1012607, nssv1012598, nssv1012671, nssv1012665, nssv1012647, nssv1012636, nssv1012639, nssv1012595, nssv1012690, nssv1012603, nssv1012623, nssv1012649, nssv1012593, nssv1012577, nssv1012572, nssv1012645, nssv1012590, nssv1012561, nssv1012622, nssv1012715, nssv1012714, nssv1012689, nssv1012670, nssv1012599, nssv1012618, nssv1012651, nssv1012588, nssv1012686, nssv1012708, nssv1012578, nssv1012696, nssv1012683, nssv1012609, nssv1012591, nssv1012568, nssv1012615, nssv1012594, nssv1012664, nssv1012601, nssv1012646, nssv1012621, nssv1012661, nssv1012678, nssv1012597, nssv1012685, nssv1012567, nssv1012658, nssv1012654, nssv1012608, nssv1012586, nssv1012626, nssv1012559, nssv1012677, nssv1012630, nssv1012625, nssv1012681, nssv1012697, nssv1012576, nssv1012574, nssv1012570, nssv1012605, nssv1012660, nssv1012655, nssv1012580, nssv1012596, nssv1012587, nssv1012650, nssv1012701, nssv1012684, nssv1012620, nssv1012600, nssv1012667, nssv1012657, nssv1012604, nssv1012710, nssv1012582, nssv1012628, nssv1012716, nssv1012566, nssv1012700, nssv1012711, nssv1012707, nssv1012585, nssv1012571, nssv1012706, nssv1012631, nssv1012695, nssv1012638, nssv1012673, nssv1012611, nssv1012702, nssv1012652, nssv1012602, nssv1012573, nssv1012679, nssv1012564, nssv1012562, nssv1012592, nssv1012565, nssv1012656
Samples
Known GenesTLL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596054
Frequency
Sample Size17421
Observed Gain0
Observed Loss158
Observed Complex0
Frequencyn/a


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