nsv6629953
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:112,818
- Publication(s):Zarrei et al. 2023
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: 1900 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 1900 SVs from 90 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6629953 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 68,535,454 | 68,648,271 |
| nsv6629953 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 69,401,172 | 69,513,989 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18316277 | Remapped | Perfect | NC_000004.12:g.(?_ 68535454)_(6864827 1_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 68,535,454 | 68,648,271 |
| nssv18319421 | Remapped | Perfect | NC_000004.12:g.(?_ 68535454)_(6864827 1_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 68,535,454 | 68,648,271 |
| nssv18316277 | Submitted genomic | NC_000004.11:g.(?_ 69401172)_(6951398 9_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 69,401,172 | 69,513,989 | ||
| nssv18319421 | Submitted genomic | NC_000004.11:g.(?_ 69401172)_(6951398 9_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 69,401,172 | 69,513,989 |