nsv4379004
- 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:22,910
- 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: 522 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 518 SVs from 33 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4379004 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 155,784,537 | 155,807,446 |
| nsv4379004 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 155,014,199 | 155,037,109 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15638097 | Remapped | Good | NC_000023.11:g.(?_ 155784537)_(155807 446_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 155,784,537 | 155,807,446 |
| nssv15670362 | Remapped | Good | NC_000023.11:g.(?_ 155784537)_(155807 446_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 155,784,537 | 155,807,446 |
| nssv15638097 | Submitted genomic | NC_000023.10:g.(?_ 155014199)_(155037 109_?)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 155,014,199 | 155,037,109 | ||
| nssv15670362 | Submitted genomic | NC_000023.10:g.(?_ 155014199)_(155037 109_?)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 155,014,199 | 155,037,109 |