nsv4387409
- 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:59,747
- 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: 598 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 659 SVs from 77 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4387409 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,550,402 |
| nsv4387409 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 98,063,359 | 98,166,865 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15655181 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9755040 2_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,550,402 |
| nssv15666734 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9755040 2_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,550,402 |
| nssv15655181 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816686 5_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,166,865 | ||
| nssv15666734 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816686 5_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,166,865 |