nsv6135737
- Organism: Homo sapiens
- Study:nstd213 (Pham et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:420,002
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: 1364 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1364 SVs from 81 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6135737 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 165,646,512 | 166,066,513 |
| nsv6135737 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 166,060,000 | 166,480,001 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17682700 | copy number gain | SAMN20524656 | Sequencing | Paired-end mapping | 419 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17682700 | Remapped | Perfect | NC_000006.12:g.165 646512_166066513du p | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 165,646,512 | 166,066,513 |
| nssv17682700 | Submitted genomic | NC_000006.11:g.166 060000_166480001du p | GRCh37 (hg19) | NC_000006.11 | Chr6 | 166,060,000 | 166,480,001 |