nsv513762
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:110,614
- Publication(s):Arlt 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: 798 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 799 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 302 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv513762 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 8,626,948 | 8,737,561 |
| nsv513762 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 8,594,989 | 8,705,602 |
| nsv513762 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 8,554,989 | 8,665,602 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv627014 | insertion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv627014 | Remapped | Perfect | NC_000023.11:g.(86 26948_?)_(?_873756 1)ins110614 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 8,626,948 | 8,737,561 |
| nssv627014 | Remapped | Perfect | NC_000023.10:g.(85 94989_?)_(?_870560 2)ins110614 | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 8,594,989 | 8,705,602 |
| nssv627014 | Submitted genomic | NC_000023.9:g.(855 4989_?)_(?_8665602 )ins110614 | NCBI36 (hg18) | NC_000023.9 | ChrX | 8,554,989 | 8,665,602 |