nsv4372854
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:42,287
- Publication(s):Zarrei et al. 2019
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: 577 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 577 SVs from 83 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4372854 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 37,496,998 | 37,539,284 |
| nsv4372854 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 38,071,135 | 38,113,421 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15624973 | Remapped | Perfect | NC_000013.11:g.(?_ 37496998)_(3753928 4_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 37,496,998 | 37,539,284 |
| nssv15625564 | Remapped | Perfect | NC_000013.11:g.(?_ 37496998)_(3753928 4_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 37,496,998 | 37,539,284 |
| nssv15624973 | Submitted genomic | NC_000013.10:g.(?_ 38071135)_(3811342 1_?)del | GRCh37 (hg19) | NC_000013.10 | Chr13 | 38,071,135 | 38,113,421 | ||
| nssv15625564 | Submitted genomic | NC_000013.10:g.(?_ 38071135)_(3811342 1_?)del | GRCh37 (hg19) | NC_000013.10 | Chr13 | 38,071,135 | 38,113,421 |