nsv5574153
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,177
- Publication(s):Ebert et al. 2021
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: 415 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 411 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 254 SVs from 29 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5574153 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 76,035,312 | 76,038,488 | ||
| nsv5574153 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000007.13 | Chr7 | 75,664,630 | 75,667,806 |
| nsv5574153 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871064.1 | Chr7|NW_00 3871064.1 | 3,564,548 | 3,567,724 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17148663 | Submitted genomic | NC_000007.14:g.760 35312_76038488delA | GRCh38 (hg38) | NC_000007.14 | Chr7 | 76,035,312 | 76,038,488 | ||
| nssv17148663 | Remapped | Perfect | NW_003871064.1:g.3 564548_3567724delA | GRCh37.p13 | First Pass | NW_003871064.1 | Chr7|NW_00 3871064.1 | 3,564,548 | 3,567,724 |
| nssv17148663 | Remapped | Perfect | NC_000007.13:g.756 64630_75667806delA | GRCh37.p13 | Second Pass | NC_000007.13 | Chr7 | 75,664,630 | 75,667,806 |