nsv4435609
- Organism: Homo sapiens
- Study:nstd172 (Deng et al. 2019)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:33,000
- Publication(s):Deng et al. 2019
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: 211 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 211 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4435609 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 114,365,721 | 114,398,720 |
| nsv4435609 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000009.11 | Chr9 | 117,128,001 | 117,161,000 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15747698 | duplication | SMI041 | Sequencing | Sequence alignment | 593 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15747698 | Remapped | Perfect | NC_000009.12:g.114 365721_114398720du p | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 114,365,721 | 114,398,720 |
| nssv15747698 | Submitted genomic | NC_000009.11:g.117 128001_117161000du p | GRCh37.p13 | NC_000009.11 | Chr9 | 117,128,001 | 117,161,000 |