nsv4376129
- 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:217,786
- 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: 2283 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 2273 SVs from 96 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4376129 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 33,794,295 | 34,012,080 |
| nsv4376129 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 33,596,762 | 33,814,547 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15621292 | Remapped | Perfect | NC_000016.10:g.(?_ 33794295)_(3401208 0_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 33,794,295 | 34,012,080 |
| nssv15665574 | Remapped | Perfect | NC_000016.10:g.(?_ 33794295)_(3401208 0_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 33,794,295 | 34,012,080 |
| nssv15621292 | Submitted genomic | NC_000016.9:g.(?_3 3596762)_(33814547 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 33,596,762 | 33,814,547 | ||
| nssv15665574 | Submitted genomic | NC_000016.9:g.(?_3 3596762)_(33814547 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 33,596,762 | 33,814,547 |