nsv959610
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:58,412
- Publication(s):Poultney 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: 580 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 580 SVs from 41 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959610 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 3,135,547 | 3,193,958 |
| nsv959610 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 3,135,545 | 3,193,956 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021312 | deletion | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021312 | Remapped | Perfect | NC_000018.10:g.(31 34824_3135547)_(31 93958_3214934)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 3,134,824 | 3,135,547 | 3,193,958 | 3,214,934 |
| nssv3021312 | Submitted genomic | NC_000018.9:g.(313 4822_3135545)_(319 3956_3214932)del | GRCh37 (hg19) | NC_000018.9 | Chr18 | 3,134,822 | 3,135,545 | 3,193,956 | 3,214,932 |