nsv949036
- Organism: Homo sapiens
- Study:nstd85 (vanSilfhout et al. 2013)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:589,179
- Publication(s):Vulto-van Silfhout et al. 2013
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: 1498 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1498 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 76 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv949036 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 133,208,789 | 133,797,967 |
| nsv949036 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 133,078,684 | 133,667,862 |
| nsv949036 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 132,583,894 | 133,173,072 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv2767645 | copy number gain | SNP array | SNP genotyping analysis | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2767645 | Remapped | Perfect | NC_000011.10:g.(?_ 133208789)_(133797 967_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 133,208,789 | 133,797,967 |
| nssv2767645 | Remapped | Perfect | NC_000011.9:g.(?_1 33078684)_(1336678 62_?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 133,078,684 | 133,667,862 |
| nssv2767645 | Submitted genomic | NC_000011.8:g.(?_1 32583894)_(1331730 72_?)dup | NCBI35 (hg17) | NC_000011.8 | Chr11 | 132,583,894 | 133,173,072 |