nsv4386165
- 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:26,421
- 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: 349 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 351 SVs from 49 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4386165 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 111,081,162 | 111,107,582 |
| nsv4386165 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 110,416,860 | 110,443,281 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15677251 | Remapped | Good | NC_000005.10:g.(?_ 111081162)_(111107 582_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 111,081,162 | 111,107,582 |
| nssv15677278 | Remapped | Good | NC_000005.10:g.(?_ 111081162)_(111107 582_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 111,081,162 | 111,107,582 |
| nssv15677251 | Submitted genomic | NC_000005.9:g.(?_1 10416860)_(1104432 81_?)dup | GRCh37 (hg19) | NC_000005.9 | Chr5 | 110,416,860 | 110,443,281 | ||
| nssv15677278 | Submitted genomic | NC_000005.9:g.(?_1 10416860)_(1104432 81_?)dup | GRCh37 (hg19) | NC_000005.9 | Chr5 | 110,416,860 | 110,443,281 |