nsv4373397
- 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:72,696
- 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: 733 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 684 SVs from 61 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4373397 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 135,723,961 | 135,796,656 |
| nsv4373397 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 134,871,801 | 134,930,645 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15695219 | copy number gain | 156892 | SNP array | Genotyping | 15 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15695219 | Remapped | Pass | NC_000023.11:g.(?_ 135723961)_(135796 656_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 135,723,961 | 135,796,656 |
| nssv15695219 | Submitted genomic | NC_000023.10:g.(?_ 134871801)_(134930 645_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 134,871,801 | 134,930,645 |