nsv949682
- 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:646,916
- 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: 4085 SVs from 113 studies. See in: genome view
Overlapping variant regions from other studies: 4085 SVs from 113 studies. See in: genome view
Overlapping variant regions from other studies: 801 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv949682 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 77,645,883 | 78,292,798 |
| nsv949682 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 78,355,600 | 79,002,515 |
| nsv949682 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 78,412,319 | 79,059,234 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv2768425 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv2768425 | Remapped | Perfect | NC_000006.12:g.(?_ 77645883)_(7829279 8_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 77,645,883 | 78,292,798 |
| nssv2768425 | Remapped | Perfect | NC_000006.11:g.(?_ 78355600)_(7900251 5_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 78,355,600 | 79,002,515 |
| nssv2768425 | Submitted genomic | NC_000006.9:g.(?_7 8412319)_(79059234 _?)dup | NCBI35 (hg17) | NC_000006.9 | Chr6 | 78,412,319 | 79,059,234 |