nsv498706
- Organism: Homo sapiens
- Study:nstd47 (Kidd et al. 2010b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:37,828
- Publication(s):Kidd et al. 2010
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: 362 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 368 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv498706 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 207,534,533 | 207,572,360 |
| nsv498706 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 207,707,878 | 207,745,705 |
| nsv498706 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 205,774,501 | 205,812,328 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv585421 | copy number loss | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv585421 | Remapped | Perfect | NC_000001.11:g.207 534533_207572360de l | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 207,534,533 | 207,572,360 |
| nssv585421 | Remapped | Perfect | NC_000001.10:g.207 707878_207745705de l | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 207,707,878 | 207,745,705 |
| nssv585421 | Submitted genomic | NC_000001.9:g.2057 74501_205812328del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 205,774,501 | 205,812,328 |