nsv5258811
- 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:41,100
- 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: 424 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 283 SVs from 44 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5258811 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000007.14 | Chr7 | 142,576,801 | 142,617,900 | ||
nsv5258811 | Remapped | Good | GRCh37.p13 | PATCHES | Second Pass | NW_003571040.1 | Chr7|NW_00 3571040.1 | 760,586 | 801,634 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16852249 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv16852249 | Submitted genomic | GRCh38.p13 | NC_000007.14 | Chr7 | 142,576,801 | 142,617,900 | ||
nssv16852249 | Remapped | Good | GRCh37.p13 | Second Pass | NW_003571040.1 | Chr7|NW_00 3571040.1 | 760,586 | 801,634 |