nsv5577123
- 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:495
- 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: 202 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 207 SVs from 30 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5577123 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 224,006,329 | 224,006,823 | ||
nsv5577123 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 224,194,031 | 224,194,525 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17062976 | Submitted genomic | NC_000001.11:g.224 006329_224006823de lC | GRCh38 (hg38) | NC_000001.11 | Chr1 | 224,006,329 | 224,006,823 | ||
nssv17062976 | Remapped | Perfect | NC_000001.10:g.224 194031_224194525de lC | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 224,194,031 | 224,194,525 |