nsv948936
- 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:351,218
- 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: 3605 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 3606 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 295 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv948936 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 683,127 | 1,034,344 |
| nsv948936 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 643,862 | 995,079 |
| nsv948936 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 613,862 | 965,079 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv2767527 | copy number loss | SNP array | SNP genotyping analysis | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2767527 | Remapped | Perfect | NC_000023.11:g.(?_ 683127)_(1034344_? )del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 683,127 | 1,034,344 |
| nssv2767527 | Remapped | Perfect | NC_000023.10:g.(?_ 643862)_(995079_?) del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 643,862 | 995,079 |
| nssv2767527 | Submitted genomic | NC_000023.8:g.(?_6 13862)_(965079_?)d el | NCBI35 (hg17) | NC_000023.8 | ChrX | 613,862 | 965,079 |