nsv949748
- Organism: Homo sapiens
- Study:nstd72 (Morak et al. 2012)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:323,702
- Publication(s):Morak et al. 2012
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: 3473 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 3474 SVs from 59 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv949748 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 1,212,766 | 1,536,467 |
| nsv949748 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 1,331,659 | 1,655,360 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv2995877 | deletion | 365 | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2995877 | Remapped | Perfect | NC_000023.11:g.121 2766_1536467del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 1,212,766 | 1,536,467 |
| nssv2995877 | Submitted genomic | NC_000023.10:g.133 1659_1655360del | GRCh37 (hg19) | NC_000023.10 | ChrX | 1,331,659 | 1,655,360 |