nsv1722
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:44,851
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 311 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 311 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 19 SVs from 8 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1722 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 5,031,097 | 5,075,947 |
| nsv1722 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 5,081,098 | 5,125,948 |
| nsv1722 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 5,021,099 | 5,065,949 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv7227 | Remapped | Perfect | NC_000016.10:g.(50 31097_?)_(?_507594 7)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 5,031,097 | 5,075,947 |
| nssv7227 | Remapped | Perfect | NC_000016.9:g.(508 1098_?)_(?_5125948 )del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 5,081,098 | 5,125,948 |
| nssv7227 | Submitted genomic | NC_000016.8:g.(502 1099_?)_(?_5065949 )del5410 | NCBI35 (hg17) | NC_000016.8 | Chr16 | 5,021,099 | 5,065,949 |