nsv822993
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:64,939
- Publication(s):Park et al. 2010
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: 603 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 603 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 366 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv822993 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 6,689,024 | 6,753,962 |
| nsv822993 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 6,689,137 | 6,754,075 |
| nsv822993 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 6,742,137 | 6,807,075 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1435071 | Remapped | Perfect | NC_000005.10:g.(?_ 6689024)_(6753962_ ?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 6,689,024 | 6,753,962 |
| nssv1435071 | Remapped | Perfect | NC_000005.9:g.(?_6 689137)_(6754075_? )del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 6,689,137 | 6,754,075 |
| nssv1435071 | Submitted genomic | NC_000005.8:g.(?_6 742137)_(6807075_? )del | NCBI36 (hg18) | NC_000005.8 | Chr5 | 6,742,137 | 6,807,075 |