nsv820699
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16,110
- Publication(s):Ju 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: 521 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 530 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 159 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820699 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,524,157 | 97,540,266 |
| nsv820699 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 98,146,258 | 98,156,729 |
| nsv820699 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 97,507,052 | 97,523,161 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420240 | Remapped | Perfect | NC_000002.12:g.(?_ 97524157)_(9754026 6_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,524,157 | 97,540,266 |
| nssv1420240 | Remapped | Pass | NC_000002.11:g.(?_ 98146258)_(9815672 9_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 98,146,258 | 98,156,729 |
| nssv1420240 | Submitted genomic | NC_000002.10:g.(?_ 97507052)_(9752316 1_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 97,507,052 | 97,523,161 |