nsv4384273
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:177,605
- Publication(s):Zarrei 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: 2081 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 2081 SVs from 97 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4384273 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 68,500,975 | 68,678,579 |
| nsv4384273 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 69,366,693 | 69,544,297 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15632514 | Remapped | Perfect | NC_000004.12:g.(?_ 68500975)_(6867857 9_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 68,500,975 | 68,678,579 |
| nssv15659966 | Remapped | Perfect | NC_000004.12:g.(?_ 68500975)_(6867857 9_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 68,500,975 | 68,678,579 |
| nssv15632514 | Submitted genomic | NC_000004.11:g.(?_ 69366693)_(6954429 7_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 69,366,693 | 69,544,297 | ||
| nssv15659966 | Submitted genomic | NC_000004.11:g.(?_ 69366693)_(6954429 7_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 69,366,693 | 69,544,297 |