nsv4740707
- 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:41,022
- 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: 201 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 160 SVs from 37 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4740707 | Remapped | Pass | GRCh38.p12 | Primary Assembly | Second Pass | NC_000004.12 | Chr4 | 74,416,749 | 74,457,770 |
| nsv4740707 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 75,427,378 | 75,493,262 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16259812 | deletion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16259812 | Remapped | Pass | NC_000004.12:g.744 16749_74457770del | GRCh38.p12 | Second Pass | NC_000004.12 | Chr4 | 74,416,749 | 74,457,770 |
| nssv16259812 | Submitted genomic | NC_000004.11:g.754 27378_75493262del | GRCh37 (hg19) | NC_000004.11 | Chr4 | 75,427,378 | 75,493,262 |