A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514897



Internal ID15466531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358570..35370838hg38UCSC Ensembl
Innerchr19:35849472..35861740hg19UCSC Ensembl
Innerchr19:40541312..40553580hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812269
hg1912269
hg1812269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2841678, nssv2841691, nssv2841612, nssv2841661, nssv2841665, nssv2841594, nssv2841713, nssv2841652, nssv2841602, nssv2841631, nssv2841610, nssv2841614, nssv2841650, nssv2841683, nssv2841685, nssv2841689, nssv2841659, nssv2841684, nssv2841613, nssv2841667, nssv2841620, nssv2841636, nssv2841715, nssv2841712, nssv2841694, nssv2841698, nssv2841628, nssv2841648, nssv2841680, nssv2841654, nssv2841623, nssv2841604, nssv2841606, nssv2841669, nssv2841719, nssv2841603, nssv2841672, nssv2841673, nssv2841630, nssv2841682, nssv2841608, nssv2841618, nssv2841670, nssv2841658, nssv2841649, nssv2841692, nssv2841721, nssv2841696, nssv2841720, nssv2841643, nssv2841645, nssv2841695, nssv2841605, nssv2841640, nssv2841622, nssv2841725, nssv2841621, nssv2841660, nssv2841710, nssv2841657, nssv2841709, nssv2841693, nssv2841627, nssv2841707, nssv2841646, nssv2841633, nssv2841717, nssv2841690, nssv2841697, nssv2841638, nssv2841651, nssv2841662, nssv2841597, nssv2841671, nssv2841624, nssv2841663, nssv2841722, nssv2841599, nssv2841724, nssv2841596, nssv2841679, nssv2841598, nssv2841592, nssv2841676, nssv2841664, nssv2841706, nssv2841687, nssv2841703, nssv2841644, nssv2841705, nssv2841609, nssv2841634, nssv2841677, nssv2841593, nssv2841674, nssv2841607, nssv2841639, nssv2841704, nssv2841718, nssv2841619, nssv2841668, nssv2841625, nssv2841629, nssv2841686, nssv2841655, nssv2841723, nssv2841626, nssv2841600, nssv2841666, nssv2841591, nssv2841635, nssv2841641, nssv2841688, nssv2841711, nssv2841615, nssv2841701, nssv2841637, nssv2841702, nssv2841632, nssv2841708, nssv2841653, nssv2841727, nssv2841595, nssv2841601, nssv2841642, nssv2841675, nssv2841647, nssv2841699, nssv2841716, nssv2841611, nssv2841700, nssv2841726, nssv2841617, nssv2841656, nssv2841681, nssv2841616, nssv2841714
SamplesNA07435, NA12767, NA12827, NA18621, NA12154, NA12249, NA12750, NA12344, NA07037, NA12802, NA21317, NA12801, NA18975, NA18966, NA12752, NA18612, NA12347, NA18570, NA19003, NA12264, NA12815, NA10847, NA12340, NA18545, NA18948, NA18953, NA18972, NA12828, NA18573, NA18608, NA10855, NA12776, NA10837, NA19257, NA11893, NA21361, NA12766, NA12287, NA10863, NA18632, NA12414, NA11919, NA12843, NA18998, NA18624, NA18967, NA12056, NA11839, NA12336, NA12383, NA11994, NA18635, NA18576, NA18960, NA10846, NA12864, NA18563, NA19197, NA18991, NA18636, NA12740, NA12761, NA10852, NA18547, NA11843, NA12329, NA11831, NA11894, NA11995, NA18593, NA21608, NA12777, NA12234, NA12144, NA18970, NA12751, NA21442, NA12239, NA12716, NA21525, NA12778, NA12877, NA18968, NA12275, NA18875, NA21455, NA12485, NA12872, NA18564, NA18961, NA10836, NA12283, NA18562, NA18579, NA19141, NA18940, NA11832, NA19258, NA12890, NA18582, NA12146, NA12272, NA10860, NA21439, NA18995, NA19193, NA12375, NA12812, NA19115, NA06995, NA12889, NA21389, NA10835, NA07022, NA11992, NA21366, NA19225, NA10838, NA12399, NA12045, NA10840, NA12236, NA12717, NA12874, NA18532, NA18935, NA06994, NA21391, NA12274, NA12832, NA12335, NA18555, NA19007, NA11917, NA10864, NA21494, NA07031
Known GenesFFAR3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514897
Frequency
Sample Size2366
Observed Gain0
Observed Loss137
Observed Complex0
Frequencyn/a


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