A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597723



Internal ID6984861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128711450..128713937hg38UCSC Ensembl
Innerchr3:128711450..128713937hg38UCSC Ensembl
Outerchr3:128711055..128714243hg38UCSC Ensembl
chr3:128430293..128432780hg19UCSC Ensembl
Innerchr3:128430293..128432780hg19UCSC Ensembl
Outerchr3:128429898..128433086hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382488
hg192488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11140756, essv11140714, essv11140673, essv11140659, essv11140657, essv11140646, essv11140734, essv11140748, essv11140653, essv11140744, essv11140723, essv11140725, essv11140667, essv11140733, essv11140707, essv11140678, essv11140764, essv11140668, essv11140644, essv11140758, essv11140709, essv11140655, essv11140728, essv11140737, essv11140741, essv11140674, essv11140720, essv11140722, essv11140719, essv11140679, essv11140648, essv11140724, essv11140695, essv11140710, essv11140685, essv11140753, essv11140746, essv11140687, essv11140694, essv11140732, essv11140708, essv11140726, essv11140727, essv11140767, essv11140735, essv11140747, essv11140658, essv11140730, essv11140692, essv11140752, essv11140698, essv11140743, essv11140686, essv11140713, essv11140672, essv11140649, essv11140716, essv11140661, essv11140691, essv11140717, essv11140643, essv11140662, essv11140681, essv11140765, essv11140663, essv11140696, essv11140718, essv11140680, essv11140676, essv11140660, essv11140665, essv11140749, essv11140762, essv11140742, essv11140721, essv11140706, essv11140763, essv11140745, essv11140715, essv11140669, essv11140664, essv11140641, essv11140754, essv11140670, essv11140729, essv11140761, essv11140769, essv11140684, essv11140705, essv11140757, essv11140711, essv11140701, essv11140700, essv11140712, essv11140645, essv11140755, essv11140703, essv11140654, essv11140689, essv11140759, essv11140656, essv11140647, essv11140702, essv11140642, essv11140697, essv11140683, essv11140688, essv11140738, essv11140652, essv11140666, essv11140760, essv11140699, essv11140768, essv11140693, essv11140736, essv11140731, essv11140650, essv11140766, essv11140704, essv11140739, essv11140740, essv11140671, essv11140682, essv11140675, essv11140690, essv11140677, essv11140750, essv11140651, essv11140751
SamplesHG00403, HG02614, NA19701, HG01413, HG02628, NA20543, HG01965, NA19794, HG02272, HG04229, NA20274, HG02433, NA11933, HG01970, NA19795, HG02215, HG01947, HG01518, HG01461, HG00327, HG03199, HG01341, NA19171, HG00356, NA19728, HG01997, NA19307, HG02541, NA19198, HG04144, HG02085, NA18642, NA18571, HG00369, HG02278, HG01069, NA21109, NA18868, HG01813, HG02187, HG00309, NA19722, NA18990, NA18557, NA18539, HG00743, HG01124, NA18614, NA18951, HG03697, HG02570, HG02265, NA18613, NA19657, HG00183, NA18934, HG03088, NA19175, NA18644, HG01162, HG01515, NA19327, HG02253, HG01938, NA19717, HG02108, NA20895, HG02731, HG00556, HG02887, NA18637, HG02508, HG01390, NA19654, HG01102, HG01311, HG03871, HG00404, HG02086, HG02283, NA19740, HG03634, HG01890, NA19682, HG01403, HG01936, NA19625, HG04093, NA19035, NA18546, NA19729, NA19256, HG04026, HG03539, NA19749, HG00565, HG02696, HG02064, HG00375, HG03920, HG01272, HG02982, HG02179, HG02274, NA19324, HG01260, NA19783, HG02188, HG04080, NA20906, HG02971, HG02373, NA19785, HG03896, NA19779, HG02396, HG01085, NA12830, HG03258, NA18609, HG04171, HG03538, HG01105, HG01920, NA19758, NA19312, NA18612, HG01927, HG01923
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597723
Frequency
Sample Size2504
Observed Gain0
Observed Loss129
Observed Complex0
Frequencyn/a


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