nsv5666256
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,446
- Publication(s):Ebert et al. 2021
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: 687 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 679 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5666256 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 155,548,459 | 155,552,904 | ||
| nsv5666256 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 154,778,120 | 154,782,565 |
| nsv5666256 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871103.3 | ChrX|NW_00 3871103.3 | 2,982,438 | 2,986,883 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17166324 | Submitted genomic | NC_000023.11:g.155 548459_155552904de lG | GRCh38 (hg38) | NC_000023.11 | ChrX | 155,548,459 | 155,552,904 | ||
| nssv17166324 | Remapped | Perfect | NW_003871103.3:g.2 982438_2986883delG | GRCh37.p13 | First Pass | NW_003871103.3 | ChrX|NW_00 3871103.3 | 2,982,438 | 2,986,883 |
| nssv17166324 | Remapped | Perfect | NC_000023.10:g.154 778120_154782565de lG | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 154,778,120 | 154,782,565 |