nsv5621087
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- 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: 154 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 154 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 |
---|---|---|---|---|---|---|---|---|---|
nsv5621087 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 159,966,159 | 159,966,159 | ||
nsv5621087 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 160,822,670 | 160,822,670 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17109410 | Submitted genomic | NC_000002.12:g.159 966159_159966160in s372 | GRCh38 (hg38) | NC_000002.12 | Chr2 | 159,966,159 | 159,966,159 | ||
nssv17109410 | Remapped | Perfect | NC_000002.11:g.160 822670_160822671in s372 | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 160,822,670 | 160,822,670 |