nsv4377717
- 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:1,393,546
- 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: 3256 SVs from 99 studies. See in: genome view
Overlapping variant regions from other studies: 3277 SVs from 100 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4377717 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 222,523,746 | 223,917,291 |
| nsv4377717 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 222,697,088 | 224,104,993 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15657834 | Remapped | Good | NC_000001.11:g.(?_ 222523746)_(223917 291_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 222,523,746 | 223,917,291 |
| nssv15663070 | Remapped | Good | NC_000001.11:g.(?_ 222523746)_(223917 291_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 222,523,746 | 223,917,291 |
| nssv15657834 | Submitted genomic | NC_000001.10:g.(?_ 222697088)_(224104 993_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 222,697,088 | 224,104,993 | ||
| nssv15663070 | Submitted genomic | NC_000001.10:g.(?_ 222697088)_(224104 993_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 222,697,088 | 224,104,993 |