nsv898037
- Organism: Homo sapiens
- Study:nstd71 (Xu et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:61,831
- Publication(s):Xu et al. 2011
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: 289 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 289 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 64 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 | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv898037 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 84,721,004 | 84,738,464 | 84,772,349 | 84,782,834 |
| nsv898037 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 84,432,047 | 84,449,507 | 84,483,392 | 84,493,877 |
| nsv898037 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 84,109,695 | 84,127,155 | 84,161,040 | 84,171,525 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1585701 | Remapped | Perfect | NC_000011.10:g.(84 721004_84738464)_( 84772349_84782834) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 84,721,004 | 84,738,464 | 84,772,349 | 84,782,834 |
| nssv1587485 | Remapped | Perfect | NC_000011.10:g.(84 721004_84738464)_( 84772349_84782834) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 84,721,004 | 84,738,464 | 84,772,349 | 84,782,834 |
| nssv1585701 | Remapped | Perfect | NC_000011.9:g.(844 32047_84449507)_(8 4483392_84493877)d el | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 84,432,047 | 84,449,507 | 84,483,392 | 84,493,877 |
| nssv1587485 | Remapped | Perfect | NC_000011.9:g.(844 32047_84449507)_(8 4483392_84493877)d el | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 84,432,047 | 84,449,507 | 84,483,392 | 84,493,877 |
| nssv1585701 | Submitted genomic | NC_000011.8:g.(841 09695_84127155)_(8 4161040_84171525)d el | NCBI36 (hg18) | NC_000011.8 | Chr11 | 84,109,695 | 84,127,155 | 84,161,040 | 84,171,525 | ||
| nssv1587485 | Submitted genomic | NC_000011.8:g.(841 09695_84127155)_(8 4161040_84171525)d el | NCBI36 (hg18) | NC_000011.8 | Chr11 | 84,109,695 | 84,127,155 | 84,161,040 | 84,171,525 |