nsv819659
- Organism: Homo sapiens
- Study:nstd43 (Kim et al. 2009)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,631
- Publication(s):Kim et al. 2009
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: 202 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 202 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 65 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819659 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 60,047,240 | 60,066,870 |
| nsv819659 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 60,081,144 | 60,100,774 |
| nsv819659 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 58,638,645 | 58,658,275 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418679 | copy number loss | SAMN00002681 | Oligo aCGH | Probe signal intensity | 1,333 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418679 | Remapped | Perfect | NC_000016.10:g.(?_ 60047240)_(6006687 0_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 60,047,240 | 60,066,870 |
| nssv1418679 | Remapped | Perfect | NC_000016.9:g.(?_6 0081144)_(60100774 _?)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 60,081,144 | 60,100,774 |
| nssv1418679 | Submitted genomic | NC_000016.8:g.(?_5 8638645)_(58658275 _?)del | NCBI36 (hg18) | NC_000016.8 | Chr16 | 58,638,645 | 58,658,275 |