nsv6628024
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:66,408
- 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: 648 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 648 SVs from 72 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6628024 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 240,684,041 | 240,750,448 |
| nsv6628024 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 241,623,458 | 241,689,865 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18306877 | Remapped | Perfect | NC_000002.12:g.(?_ 240684041)_(240750 448_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 240,684,041 | 240,750,448 |
| nssv18308999 | Remapped | Perfect | NC_000002.12:g.(?_ 240684041)_(240750 448_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 240,684,041 | 240,750,448 |
| nssv18306877 | Submitted genomic | NC_000002.11:g.(?_ 241623458)_(241689 865_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 241,623,458 | 241,689,865 | ||
| nssv18308999 | Submitted genomic | NC_000002.11:g.(?_ 241623458)_(241689 865_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 241,623,458 | 241,689,865 |