A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608684



Internal ID6995608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35554207..35601118hg38UCSC Ensembl
chr6:35521984..35568895hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3846912
hg1946912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12315765, essv12315706, essv12315655, essv12315692, essv12315718, essv12315699, essv12315659, essv12315773, essv12315777, essv12315768, essv12315689, essv12315748, essv12315753, essv12315766, essv12315695, essv12315654, essv12315727, essv12315737, essv12315735, essv12315757, essv12315690, essv12315738, essv12315719, essv12315660, essv12315722, essv12315656, essv12315717, essv12315703, essv12315670, essv12315676, essv12315679, essv12315762, essv12315675, essv12315688, essv12315759, essv12315740, essv12315732, essv12315721, essv12315701, essv12315754, essv12315657, essv12315716, essv12315772, essv12315685, essv12315666, essv12315705, essv12315775, essv12315681, essv12315724, essv12315725, essv12315652, essv12315664, essv12315767, essv12315769, essv12315764, essv12315755, essv12315687, essv12315750, essv12315770, essv12315696, essv12315691, essv12315693, essv12315684, essv12315645, essv12315742, essv12315723, essv12315697, essv12315730, essv12315739, essv12315746, essv12315644, essv12315673, essv12315709, essv12315700, essv12315756, essv12315649, essv12315728, essv12315647, essv12315729, essv12315707, essv12315714, essv12315661, essv12315667, essv12315712, essv12315771, essv12315674, essv12315671, essv12315743, essv12315713, essv12315708, essv12315648, essv12315704, essv12315650, essv12315760, essv12315651, essv12315715, essv12315680, essv12315758, essv12315778, essv12315668, essv12315745, essv12315731, essv12315702, essv12315698, essv12315734, essv12315747, essv12315669, essv12315658, essv12315686, essv12315736, essv12315677, essv12315720, essv12315761, essv12315774, essv12315744, essv12315749, essv12315763, essv12315711, essv12315662, essv12315663, essv12315726, essv12315683, essv12315694, essv12315776, essv12315733, essv12315665, essv12315672, essv12315710, essv12315678, essv12315682, essv12315751, essv12315752, essv12315653, essv12315741, essv12315646, essv12315643
SamplesHG04212, HG01413, HG03857, HG01098, HG01918, HG03652, HG01303, HG03228, HG03965, HG03731, HG01961, HG03960, HG00358, HG03687, HG03753, HG02784, HG02648, HG04202, HG03738, HG02122, HG04211, HG03717, HG02661, HG04002, NA19795, HG04094, HG01305, HG02476, HG03668, HG03963, HG04018, HG03895, HG03667, HG02536, HG03944, HG03999, HG03679, HG04100, HG02690, HG04022, HG03757, HG04206, HG01968, HG02549, HG03874, HG03663, HG03479, HG01840, HG02603, HG01242, HG02278, HG01893, HG02252, HG03986, HG04106, HG01176, HG04047, HG02477, HG01967, HG04075, HG03862, HG01164, HG03697, HG02439, HG03861, HG03685, HG02793, HG02075, HG02345, HG04039, HG01162, HG04107, HG03711, HG02775, HG03491, HG04035, HG04019, HG01077, HG01852, HG01049, HG04235, HG02789, HG00740, HG01390, HG01777, HG03660, HG02577, HG03974, HG03643, HG04017, HG01101, HG03971, HG03745, HG03634, HG02724, HG03672, HG04093, HG02127, HG03694, HG01992, NA21087, HG04025, HG03848, HG02557, HG01954, HG04026, HG02010, HG03708, HG02546, HG03949, HG03838, HG02790, HG03695, HG01396, HG01977, HG03702, HG01974, HG02580, HG04003, HG03703, HG01917, HG03896, HG03977, HG03849, HG01089, HG01600, HG03872, HG02681, HG02348, HG02774, HG03856, HG04056, HG03867, HG03686, HG01061, HG01976
Known GenesFKBP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608684
Frequency
Sample Size2504
Observed Gain0
Observed Loss136
Observed Complex0
Frequencyn/a


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