nsv1046695
- Organism: Homo sapiens
- Study:nstd100 (Coe et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:19
- Validation:Not tested
- Clinical Assertions: No
- Region Size:251,227
- Publication(s):Coe et al. 2014
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 934 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 930 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 271 SVs from 25 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv1046695 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nsv1046695 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nsv1046695 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3507512 | copy number gain | SNP array | Probe signal intensity |
nssv3509098 | copy number gain | SNP array | Probe signal intensity |
nssv3509890 | copy number gain | SNP array | Probe signal intensity |
nssv3510794 | copy number gain | SNP array | Probe signal intensity |
nssv3512607 | copy number gain | SNP array | Probe signal intensity |
nssv3515113 | copy number gain | SNP array | Probe signal intensity |
nssv3516014 | copy number gain | SNP array | Probe signal intensity |
nssv3516887 | copy number gain | SNP array | Probe signal intensity |
nssv3518879 | copy number gain | SNP array | Probe signal intensity |
nssv3518896 | copy number loss | SNP array | Probe signal intensity |
nssv3519774 | copy number gain | SNP array | Probe signal intensity |
nssv3521397 | copy number gain | SNP array | Probe signal intensity |
nssv3521720 | copy number gain | SNP array | Probe signal intensity |
nssv3710627 | copy number gain | SNP array | Probe signal intensity |
nssv3710628 | copy number gain | SNP array | Probe signal intensity |
nssv3710629 | copy number gain | SNP array | Probe signal intensity |
nssv3710630 | copy number gain | SNP array | Probe signal intensity |
nssv3710631 | copy number gain | SNP array | Probe signal intensity |
nssv3710632 | copy number gain | SNP array | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv3507512 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3509098 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3509890 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3510794 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3512607 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3515113 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3516014 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3516887 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3518879 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3518896 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3519774 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3521397 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3521720 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3710627 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3710628 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3710629 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3710630 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3710631 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3710632 | Remapped | Perfect | NC_000011.10:g.(?_ 67730549)_(6798177 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,730,549 | 67,981,775 |
nssv3507512 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3509098 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3509890 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3510794 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3512607 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3515113 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3516014 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3516887 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3518879 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3518896 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3519774 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3521397 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3521720 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3710627 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3710628 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3710629 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3710630 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3710631 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3710632 | Remapped | Perfect | NC_000011.9:g.(?_6 7498020)_(67749246 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 67,498,020 | 67,749,246 |
nssv3507512 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3509098 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3509890 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3510794 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3512607 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3515113 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3516014 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3516887 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3518879 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3518896 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3519774 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3521397 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3521720 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3710627 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3710628 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3710629 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3710630 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3710631 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 | ||
nssv3710632 | Submitted genomic | NC_000011.8:g.(?_6 7254596)_(67505822 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 67,254,596 | 67,505,822 |