nsv4373138
- 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:562,242
- 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: 2937 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 3075 SVs from 102 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4373138 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 21,943,052 | 22,505,293 |
| nsv4373138 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 22,411,243 | 22,974,280 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15672198 | Remapped | Good | NC_000014.9:g.(?_2 1943052)_(22505293 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 21,943,052 | 22,505,293 |
| nssv15697620 | Remapped | Good | NC_000014.9:g.(?_2 1943052)_(22505293 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 21,943,052 | 22,505,293 |
| nssv15672198 | Submitted genomic | NC_000014.8:g.(?_2 2411243)_(22974280 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 22,411,243 | 22,974,280 | ||
| nssv15697620 | Submitted genomic | NC_000014.8:g.(?_2 2411243)_(22974280 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 22,411,243 | 22,974,280 |