nsv5598863
- 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:5,578
- 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: 209 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 209 SVs from 49 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5598863 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000019.10 | Chr19 | 46,119,477 | 46,125,054 | ||
nsv5598863 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 46,622,734 | 46,628,311 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv17105422 | deletion | SAMN00801888 | Sequencing | Sequence alignment | 2,004 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17105422 | Submitted genomic | NC_000019.10:g.461 19477_46125054delA | GRCh38 (hg38) | NC_000019.10 | Chr19 | 46,119,477 | 46,125,054 | ||
nssv17105422 | Remapped | Perfect | NC_000019.9:g.4662 2734_46628311delA | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 46,622,734 | 46,628,311 |