nsv983741
- Organism: Homo sapiens
- Study:nstd82 (Sudmant et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:22,624
- Publication(s):Sudmant et al. 2013
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: 436 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 436 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 168 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv983741 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 57,293,349 | 57,315,972 |
| nsv983741 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 57,867,483 | 57,890,106 |
| nsv983741 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 56,765,484 | 56,788,107 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| nssv2757152 | deletion | HGDP01284 | Sequencing | Read depth | 1 | 17,196 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2757152 | Remapped | Perfect | NC_000013.11:g.(?_ 57293349)_(5731597 2_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 57,293,349 | 57,315,972 |
| nssv2757152 | Remapped | Perfect | NC_000013.10:g.(?_ 57867483)_(5789010 6_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 57,867,483 | 57,890,106 |
| nssv2757152 | Submitted genomic | NC_000013.9:g.(?_5 6765484)_(56788107 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 56,765,484 | 56,788,107 |