nsv5292086
- 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:57,300
- 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: 383 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 383 SVs from 50 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5292086 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000019.10 | Chr19 | 36,410,501 | 36,467,800 | ||
nsv5292086 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 36,901,403 | 36,958,702 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16821070 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv16821070 | Submitted genomic | GRCh38.p13 | NC_000019.10 | Chr19 | 36,410,501 | 36,467,800 | ||
nssv16821070 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 36,901,403 | 36,958,702 |