nsv6314778
- Organism: Homo sapiens
- Study:nstd220 (Chen et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,428,573
- Publication(s):Chen et al. 2022
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: 16343 SVs from 131 studies. See in: genome view
Overlapping variant regions from other studies: 16346 SVs from 131 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 |
---|---|---|---|---|---|---|---|---|---|
nsv6314778 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 23,745,809 | 28,174,381 |
nsv6314778 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 23,990,956 | 28,419,527 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17976212 | copy number gain | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17976212 | Remapped | Perfect | NC_000015.10:g.(23 745809_?)_(?_28174 381)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 23,745,809 | 28,174,381 |
nssv17976212 | Submitted genomic | NC_000015.9:g.(239 90956_?)_(?_284195 27)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 23,990,956 | 28,419,527 |