nsv4376889
- 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:467,691
- 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: 2796 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 2932 SVs from 101 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4376889 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 22,041,843 | 22,509,533 |
| nsv4376889 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 22,510,089 | 22,978,516 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15651867 | Remapped | Good | NC_000014.9:g.(?_2 2041843)_(22509533 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 22,041,843 | 22,509,533 |
| nssv15666314 | Remapped | Good | NC_000014.9:g.(?_2 2041843)_(22509533 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 22,041,843 | 22,509,533 |
| nssv15651867 | Submitted genomic | NC_000014.8:g.(?_2 2510089)_(22978516 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 22,510,089 | 22,978,516 | ||
| nssv15666314 | Submitted genomic | NC_000014.8:g.(?_2 2510089)_(22978516 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 22,510,089 | 22,978,516 |