nsv6635187
- Organism: Homo sapiens
- Study:nstd227 (Kikas 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:2,805,804
- Publication(s):Kikas 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: 12573 SVs from 119 studies. See in: genome view
Overlapping variant regions from other studies: 10991 SVs from 118 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6635187 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 32,154,461 | 34,960,264 |
| nsv6635187 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 32,165,782 | 34,194,635 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18327579 | deletion | SNP array | Probe signal intensity |
| nssv18327581 | deletion | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18327579 | Remapped | Pass | NC_000016.10:g.(32 154461_?)_(?_34960 264)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,154,461 | 34,960,264 |
| nssv18327581 | Remapped | Pass | NC_000016.10:g.(32 154461_?)_(?_34960 264)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,154,461 | 34,960,264 |
| nssv18327579 | Submitted genomic | NC_000016.9:g.(321 65782_?)_(?_341946 35)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 32,165,782 | 34,194,635 | ||
| nssv18327581 | Submitted genomic | NC_000016.9:g.(321 65782_?)_(?_341946 35)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 32,165,782 | 34,194,635 |