nsv1159698
- Organism: Homo sapiens
- Study:nstd106 (Alsmadi et al. 2014)
- Variant Type:translocation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Alsmadi 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: 206 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 205 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 197 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv1159698 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 196,934 | 196,934 | not reported |
| nsv1159698 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 197,309 | 197,309 | not reported |
| nsv1159698 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 242,874 | 242,874 | not reported | ||
| nsv1159698 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 243,249 | 243,249 | not reported |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4024763 | intrachromosomal translocation | KWS2 | Sequencing | Read depth and paired-end mapping | 21,718 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv4024763 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 196,934 | 196,934 | not reported |
| nssv4024763 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 197,309 | 197,309 | not reported |
| nssv4024763 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 242,874 | 242,874 | not reported | ||
| nssv4024763 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 243,249 | 243,249 | not reported |