nsv5240991
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,000
- Publication(s):Chen 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: 146 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 146 SVs from 34 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5240991 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000009.12 | Chr9 | 87,728,101 | 87,735,100 | ||
nsv5240991 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 90,343,016 | 90,350,015 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16857391 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv16857391 | Submitted genomic | GRCh38.p13 | NC_000009.12 | Chr9 | 87,728,101 | 87,735,100 | ||
nssv16857391 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 90,343,016 | 90,350,015 |