nsv7098711
- Organism: Homo sapiens
- Study:nstd230 (Sugimoto et al. 2023)
- Variant Type:complex chromosomal rearrangement
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:17
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
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: 144 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 130 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 130 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 152 SVs from 17 studies. See in: genome view
Overlapping variant regions from other studies: 152 SVs from 17 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 130 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 130 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 244 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 152 SVs from 17 studies. See in: genome view
Overlapping variant regions from other studies: 152 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 122,973,961 | 122,973,961 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 122,973,983 | 122,973,983 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 123,022,190 | 123,022,190 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 123,022,190 | 123,022,190 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,023,011 | 124,023,011 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,023,012 | 124,023,012 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,750,045 | 124,750,045 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,751,276 | 124,751,276 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,753,575 | 124,753,575 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,753,576 | 124,753,576 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,762,502 | 124,762,502 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,762,502 | 124,762,502 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,800,523 | 124,800,523 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,800,566 | 124,800,566 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,822,816 | 124,822,816 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 124,822,827 | 124,822,827 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 125,850,169 | 125,850,169 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 125,850,170 | 125,850,170 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 126,181,125 | 126,181,125 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 126,181,127 | 126,181,127 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 127,439,977 | 127,439,977 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 127,440,026 | 127,440,026 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 127,440,156 | 127,440,156 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 127,440,161 | 127,440,161 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 127,458,812 | 127,458,812 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 127,458,812 | 127,458,812 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 150,720,493 | 150,720,493 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 150,720,494 | 150,720,494 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 2,791,486 | 2,791,486 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 2,791,873 | 2,791,873 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 6,134,051 | 6,134,051 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 6,134,052 | 6,134,052 | - |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 38,119,728 | 38,119,728 | + |
| nsv7098711 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 38,119,730 | 38,119,730 | - |
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 123,731,537 | 123,731,537 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 123,731,559 | 123,731,559 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 123,779,766 | 123,779,766 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 123,779,766 | 123,779,766 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 124,780,588 | 124,780,588 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 124,780,589 | 124,780,589 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,507,622 | 125,507,622 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,508,853 | 125,508,853 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,511,152 | 125,511,152 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,511,153 | 125,511,153 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,520,079 | 125,520,079 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,520,079 | 125,520,079 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,558,100 | 125,558,100 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,558,143 | 125,558,143 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,580,393 | 125,580,393 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 125,580,404 | 125,580,404 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 126,607,746 | 126,607,746 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 126,607,747 | 126,607,747 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 126,938,702 | 126,938,702 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 126,938,704 | 126,938,704 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 128,197,553 | 128,197,553 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 128,197,602 | 128,197,602 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 128,197,732 | 128,197,732 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 128,197,737 | 128,197,737 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 128,216,388 | 128,216,388 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 128,216,388 | 128,216,388 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 151,577,007 | 151,577,007 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 151,577,008 | 151,577,008 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 2,833,678 | 2,833,678 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 2,834,065 | 2,834,065 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 6,176,014 | 6,176,014 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 6,176,015 | 6,176,015 | - | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 35,699,692 | 35,699,692 | + | ||
| nsv7098711 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 35,699,694 | 35,699,694 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18792468 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792472 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792469 | interchromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792473 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792474 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792475 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792477 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792478 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792483 | interchromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792482 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792476 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792479 | interchromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792470 | interchromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792471 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792481 | intrachromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792484 | interchromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
| nssv18792480 | interchromosomal translocation | FHU18-163 | Sequencing | Sequence alignment | 17 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv18792468 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 122,973,961 | 122,973,961 | + |
| nssv18792472 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 122,973,983 | 122,973,983 | - |
| nssv18792469 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 123,022,190 | 123,022,190 | - |
| nssv18792473 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 123,022,190 | 123,022,190 | + |
| nssv18792474 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,023,011 | 124,023,011 | - |
| nssv18792468 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,023,012 | 124,023,012 | + |
| nssv18792475 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,750,045 | 124,750,045 | + |
| nssv18792477 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,751,276 | 124,751,276 | - |
| nssv18792473 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,753,575 | 124,753,575 | - |
| nssv18792478 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,753,576 | 124,753,576 | + |
| nssv18792474 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,762,502 | 124,762,502 | + |
| nssv18792483 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,762,502 | 124,762,502 | - |
| nssv18792482 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,800,523 | 124,800,523 | + |
| nssv18792476 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,800,566 | 124,800,566 | - |
| nssv18792475 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,822,816 | 124,822,816 | + |
| nssv18792479 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 124,822,827 | 124,822,827 | - |
| nssv18792470 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 125,850,169 | 125,850,169 | - |
| nssv18792478 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 125,850,170 | 125,850,170 | + |
| nssv18792471 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 126,181,125 | 126,181,125 | + |
| nssv18792481 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 126,181,127 | 126,181,127 | - |
| nssv18792476 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 127,439,977 | 127,439,977 | - |
| nssv18792477 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 127,440,026 | 127,440,026 | + |
| nssv18792472 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 127,440,156 | 127,440,156 | - |
| nssv18792482 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 127,440,161 | 127,440,161 | + |
| nssv18792471 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 127,458,812 | 127,458,812 | + |
| nssv18792481 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 127,458,812 | 127,458,812 | - |
| nssv18792484 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,720,493 | 150,720,493 | + |
| nssv18792480 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,720,494 | 150,720,494 | - |
| nssv18792469 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 2,791,486 | 2,791,486 | - |
| nssv18792470 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 2,791,873 | 2,791,873 | + |
| nssv18792479 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 6,134,051 | 6,134,051 | + |
| nssv18792483 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 6,134,052 | 6,134,052 | - |
| nssv18792480 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 38,119,728 | 38,119,728 | + |
| nssv18792484 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 38,119,730 | 38,119,730 | - |
| nssv18792468 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 123,731,537 | 123,731,537 | + | ||
| nssv18792472 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 123,731,559 | 123,731,559 | - | ||
| nssv18792469 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 123,779,766 | 123,779,766 | - | ||
| nssv18792473 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 123,779,766 | 123,779,766 | + | ||
| nssv18792474 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 124,780,588 | 124,780,588 | - | ||
| nssv18792468 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 124,780,589 | 124,780,589 | + | ||
| nssv18792475 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,507,622 | 125,507,622 | + | ||
| nssv18792477 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,508,853 | 125,508,853 | - | ||
| nssv18792473 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,511,152 | 125,511,152 | - | ||
| nssv18792478 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,511,153 | 125,511,153 | + | ||
| nssv18792474 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,520,079 | 125,520,079 | + | ||
| nssv18792483 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,520,079 | 125,520,079 | - | ||
| nssv18792482 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,558,100 | 125,558,100 | + | ||
| nssv18792476 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,558,143 | 125,558,143 | - | ||
| nssv18792475 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,580,393 | 125,580,393 | + | ||
| nssv18792479 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 125,580,404 | 125,580,404 | - | ||
| nssv18792470 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 126,607,746 | 126,607,746 | - | ||
| nssv18792478 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 126,607,747 | 126,607,747 | + | ||
| nssv18792471 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 126,938,702 | 126,938,702 | + | ||
| nssv18792481 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 126,938,704 | 126,938,704 | - | ||
| nssv18792476 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 128,197,553 | 128,197,553 | - | ||
| nssv18792477 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 128,197,602 | 128,197,602 | + | ||
| nssv18792472 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 128,197,732 | 128,197,732 | - | ||
| nssv18792482 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 128,197,737 | 128,197,737 | + | ||
| nssv18792471 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 128,216,388 | 128,216,388 | + | ||
| nssv18792481 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 128,216,388 | 128,216,388 | - | ||
| nssv18792484 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 151,577,007 | 151,577,007 | + | ||
| nssv18792480 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 151,577,008 | 151,577,008 | - | ||
| nssv18792469 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 2,833,678 | 2,833,678 | - | ||
| nssv18792470 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 2,834,065 | 2,834,065 | + | ||
| nssv18792479 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 6,176,014 | 6,176,014 | + | ||
| nssv18792483 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 6,176,015 | 6,176,015 | - | ||
| nssv18792480 | Submitted genomic | GRCh37 (hg19) | NC_000018.9 | Chr18 | 35,699,692 | 35,699,692 | + | ||
| nssv18792484 | Submitted genomic | GRCh37 (hg19) | NC_000018.9 | Chr18 | 35,699,694 | 35,699,694 | - |