nsv5209360
- 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:7,500
- 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: 140 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 51 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5209360 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000003.12 | Chr3 | 46,660,201 | 46,667,700 | ||
nsv5209360 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 46,701,691 | 46,709,190 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16856396 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv16856396 | Submitted genomic | GRCh38.p13 | NC_000003.12 | Chr3 | 46,660,201 | 46,667,700 | ||
nssv16856396 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 46,701,691 | 46,709,190 |