nsv4433640
- Organism: Homo sapiens
- Study:nstd172 (Deng et al. 2019)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:38,317
- Publication(s):Deng et al. 2019
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: 408 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 408 SVs from 59 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4433640 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 172,128,295 | 172,166,611 |
| nsv4433640 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000002.11 | Chr2 | 172,993,023 | 173,031,339 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15749359 | deletion | SMI034 | Sequencing | Sequence alignment | 578 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15749359 | Remapped | Perfect | NC_000002.12:g.172 128295_172166611de l | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 172,128,295 | 172,166,611 |
| nssv15749359 | Submitted genomic | NC_000002.11:g.172 993023_173031339de l | GRCh37.p13 | NC_000002.11 | Chr2 | 172,993,023 | 173,031,339 |