nsv4736781
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:99,512,215
- Publication(s):Quan et al. 2021
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: 261763 SVs from 148 studies. See in: genome view
Overlapping variant regions from other studies: 260710 SVs from 148 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4736781 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 25,804,388 | 125,316,602 |
| nsv4736781 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 25,957,322 | 125,801,148 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16294728 | deletion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16294728 | Remapped | Good | NC_000012.12:g.258 04388_125316602del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 25,804,388 | 125,316,602 |
| nssv16294728 | Submitted genomic | NC_000012.11:g.259 57322_125801148del | GRCh37 (hg19) | NC_000012.11 | Chr12 | 25,957,322 | 125,801,148 |