nsv7099292
- Organism: Homo sapiens
- Study:nstd231 (Ali et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:29,630
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: 213 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 213 SVs from 32 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7099292 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 93,838,068 | 93,867,697 |
| nsv7099292 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 94,490,321 | 94,519,950 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18793006 | duplication | SNP array | SNP genotyping analysis |
| nssv18793039 | duplication | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18793006 | Remapped | Perfect | NC_000013.11:g.(93 838068_?)_(?_93867 697)dup | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 93,838,068 | 93,867,697 |
| nssv18793039 | Remapped | Perfect | NC_000013.11:g.(93 838068_?)_(?_93867 697)dup | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 93,838,068 | 93,867,697 |
| nssv18793006 | Submitted genomic | NC_000013.10:g.(94 490321_?)_(?_94519 950)dup | GRCh37 (hg19) | NC_000013.10 | Chr13 | 94,490,321 | 94,519,950 | ||
| nssv18793039 | Submitted genomic | NC_000013.10:g.(94 490321_?)_(?_94519 950)dup | GRCh37 (hg19) | NC_000013.10 | Chr13 | 94,490,321 | 94,519,950 |