nsv6632510
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:14,919
- Publication(s):Zarrei et al. 2023
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: 484 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 424 SVs from 47 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6632510 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 143,910,788 | 143,925,706 |
| nsv6632510 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 144,984,956 | 144,999,874 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18285192 | Remapped | Perfect | NC_000008.11:g.(?_ 143910788)_(143925 706_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 143,910,788 | 143,925,706 |
| nssv18298134 | Remapped | Perfect | NC_000008.11:g.(?_ 143910788)_(143925 706_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 143,910,788 | 143,925,706 |
| nssv18285192 | Submitted genomic | NC_000008.10:g.(?_ 144984956)_(144999 874_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 144,984,956 | 144,999,874 | ||
| nssv18298134 | Submitted genomic | NC_000008.10:g.(?_ 144984956)_(144999 874_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 144,984,956 | 144,999,874 |