nsv6623640
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:351,192
- Publication(s):Zarrei et al. 2023
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: 1521 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1521 SVs from 84 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6623640 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 29,655,415 | 30,006,606 |
| nsv6623640 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 29,666,736 | 30,017,927 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18299821 | duplication | OSC5160 | SNP array | Probe signal intensity | nssv18299509, nssv18298941, nssv18298940 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18299821 | Remapped | Perfect | NC_000016.10:g.(?_ 29655415)_(3000660 6_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 29,655,415 | 30,006,606 |
| nssv18299821 | Submitted genomic | NC_000016.9:g.(?_2 9666736)_(30017927 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 29,666,736 | 30,017,927 |