nsv1392336
- Organism: Homo sapiens
- Study:nstd122 (Duyzend et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:4
- Validation:Not tested
- Clinical Assertions: No
- Region Size:167,160
- Publication(s):Duyzend et al. 2015
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: 2398 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 2359 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 889 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1392336 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 10,646,837 | 10,813,996 |
| nsv1392336 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 10,698,461 | 10,865,620 |
| nsv1392336 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 9,720,332 | 9,887,491 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv8109443 | copy number loss | SNP array | Probe signal intensity |
| nssv8606568 | copy number gain | SNP array | Probe signal intensity |
| nssv8608341 | copy number loss | SNP array | Probe signal intensity |
| nssv8611065 | copy number loss | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv8109443 | Remapped | Perfect | NC_000021.9:g.(?_1 0646837)_(10813996 _?)del | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 10,646,837 | 10,813,996 |
| nssv8606568 | Remapped | Perfect | NC_000021.9:g.(?_1 0646837)_(10813996 _?)dup | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 10,646,837 | 10,813,996 |
| nssv8608341 | Remapped | Perfect | NC_000021.9:g.(?_1 0646837)_(10813996 _?)del | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 10,646,837 | 10,813,996 |
| nssv8611065 | Remapped | Perfect | NC_000021.9:g.(?_1 0646837)_(10813996 _?)del | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 10,646,837 | 10,813,996 |
| nssv8109443 | Remapped | Perfect | NC_000021.8:g.(?_1 0698461)_(10865620 _?)del | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 10,698,461 | 10,865,620 |
| nssv8606568 | Remapped | Perfect | NC_000021.8:g.(?_1 0698461)_(10865620 _?)dup | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 10,698,461 | 10,865,620 |
| nssv8608341 | Remapped | Perfect | NC_000021.8:g.(?_1 0698461)_(10865620 _?)del | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 10,698,461 | 10,865,620 |
| nssv8611065 | Remapped | Perfect | NC_000021.8:g.(?_1 0698461)_(10865620 _?)del | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 10,698,461 | 10,865,620 |
| nssv8109443 | Submitted genomic | NC_000021.7:g.(?_9 720332)_(9887491_? )del | NCBI36 (hg18) | NC_000021.7 | Chr21 | 9,720,332 | 9,887,491 | ||
| nssv8606568 | Submitted genomic | NC_000021.7:g.(?_9 720332)_(9887491_? )dup | NCBI36 (hg18) | NC_000021.7 | Chr21 | 9,720,332 | 9,887,491 | ||
| nssv8608341 | Submitted genomic | NC_000021.7:g.(?_9 720332)_(9887491_? )del | NCBI36 (hg18) | NC_000021.7 | Chr21 | 9,720,332 | 9,887,491 | ||
| nssv8611065 | Submitted genomic | NC_000021.7:g.(?_9 720332)_(9887491_? )del | NCBI36 (hg18) | NC_000021.7 | Chr21 | 9,720,332 | 9,887,491 |