nsv4388378
- 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:26,258
- 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: 1049 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 1049 SVs from 78 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4388378 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 1,467,526 | 1,493,783 |
| nsv4388378 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 1,402,906 | 1,429,163 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15634720 | Remapped | Perfect | NC_000001.11:g.(?_ 1467526)_(1493783_ ?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 1,467,526 | 1,493,783 |
| nssv15655095 | Remapped | Perfect | NC_000001.11:g.(?_ 1467526)_(1493783_ ?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 1,467,526 | 1,493,783 |
| nssv15634720 | Submitted genomic | NC_000001.10:g.(?_ 1402906)_(1429163_ ?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 1,402,906 | 1,429,163 | ||
| nssv15655095 | Submitted genomic | NC_000001.10:g.(?_ 1402906)_(1429163_ ?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 1,402,906 | 1,429,163 |