nsv5579864
- Organism: Homo sapiens
- Study:nstd207 (Ebert 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:549
- Publication(s):Ebert 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: 122 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 27 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5579864 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 77,042,651 | 77,043,199 | ||
nsv5579864 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 76,338,476 | 76,339,024 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17148516 | Submitted genomic | NC_000005.10:g.770 42651_77043199delA | GRCh38 (hg38) | NC_000005.10 | Chr5 | 77,042,651 | 77,043,199 | ||
nssv17148516 | Remapped | Perfect | NC_000005.9:g.7633 8476_76339024delA | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 76,338,476 | 76,339,024 |