nsv4387453
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:77,189
- 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: 729 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 724 SVs from 58 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4387453 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 155,646,259 | 155,723,447 |
| nsv4387453 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 154,875,920 | 154,953,109 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15661684 | copy number loss | 4-0032-001 | SNP array | Genotyping | 39 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15661684 | Remapped | Good | NC_000023.11:g.(?_ 155646259)_(155723 447_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 155,646,259 | 155,723,447 |
| nssv15661684 | Submitted genomic | NC_000023.10:g.(?_ 154875920)_(154953 109_?)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 154,875,920 | 154,953,109 |