nsv6315588
- Organism: Homo sapiens
- Study:nstd222 (Bzdega et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:741,388
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: 2649 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 2649 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6315588 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 85,952,700 | 86,694,087 | ||
| nsv6315588 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 85,986,306 | 86,727,693 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv17977124 | copy number loss | LLDD006.3 | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17977124 | Submitted genomic | NC_000016.10:g.(85 952700_?)_(?_86694 087)del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 85,952,700 | 86,694,087 | ||
| nssv17977124 | Remapped | Perfect | NC_000016.9:g.(859 86306_?)_(?_867276 93)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 85,986,306 | 86,727,693 |