nsv6026959
- Organism: Homo sapiens
- Study:nstd212 (Wu 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:260,894
- Publication(s):Wu 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: 1116 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 1116 SVs from 80 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6026959 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 101,161,539 | 101,422,432 | ||
| nsv6026959 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 101,813,890 | 102,074,783 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17612954 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17612954 | Submitted genomic | NC_000013.11:g.101 161539_101422432du p | GRCh38 (hg38) | NC_000013.11 | Chr13 | 101,161,539 | 101,422,432 | ||
| nssv17612954 | Remapped | Perfect | NC_000013.10:g.101 813890_102074783du p | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 101,813,890 | 102,074,783 |