nsv1158568
- 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: 88 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 272 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 88 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 278 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv1158568 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 53,865,585 | 53,865,585 | - |
| nsv1158568 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 19,054,415 | 19,054,415 | - |
| nsv1158568 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 53,933,278 | 53,933,278 | - | ||
| nsv1158568 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 19,054,413 | 19,054,413 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4025986 | interchromosomal translocation | KWS1 | Sequencing | Read depth and paired-end mapping | 22,470 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv4025986 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 53,865,585 | 53,865,585 | - |
| nssv4025986 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 19,054,415 | 19,054,415 | - |
| nssv4025986 | Submitted genomic | GRCh37 (hg19) | NC_000007.13 | Chr7 | 53,933,278 | 53,933,278 | - | ||
| nssv4025986 | Submitted genomic | GRCh37 (hg19) | NC_000009.11 | Chr9 | 19,054,413 | 19,054,413 | - |