nsv6132644
- Organism: Homo sapiens
- Study:nstd213 (Pham et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,750,005
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: 44232 SVs from 128 studies. See in: genome view
Overlapping variant regions from other studies: 44233 SVs from 128 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6132644 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 38,255,863 | 56,005,867 |
| nsv6132644 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 38,830,000 | 56,580,001 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17677749 | copy number loss | SAMN20524656 | Sequencing | Paired-end mapping | 419 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17677749 | Remapped | Perfect | NC_000013.11:g.382 55863_56005867del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 38,255,863 | 56,005,867 |
| nssv17677749 | Submitted genomic | NC_000013.10:g.388 30000_56580001del | GRCh37 (hg19) | NC_000013.10 | Chr13 | 38,830,000 | 56,580,001 |