nsv3060331
- Organism: Homo sapiens
- Study:nstd140 (Fan et al. 2017)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:11,484
- Publication(s):Fan et al. 2017
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: 298 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 298 SVs from 56 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3060331 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 89,762,532 | 89,774,015 |
| nsv3060331 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 89,495,700 | 89,507,183 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14021855 | deletion | CHM1 | Sequencing | Local sequence assembly | 7,551 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14021855 | Remapped | Perfect | NC_000011.10:g.897 62532_89774015del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 89,762,532 | 89,774,015 |
| nssv14021855 | Submitted genomic | NC_000011.9:g.8949 5700_89507183del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 89,495,700 | 89,507,183 |