nsv515483
- Organism: Homo sapiens
- Study:nstd55 (Zhu et al. 2011)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,963
- Publication(s):Zhu et al. 2011
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: 611 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 611 SVs from 51 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv515483 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 140,412,830 | 140,420,792 |
| nsv515483 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 139,494,995 | 139,502,957 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv650721 | deletion | PAT473 | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv650721 | Remapped | Perfect | NC_000023.11:g.140 412830_140420792de l | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 140,412,830 | 140,420,792 |
| nssv650721 | Submitted genomic | NC_000023.10:g.139 494995_139502957de l | GRCh37 (hg19) | NC_000023.10 | ChrX | 139,494,995 | 139,502,957 |