nsv5945032
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:51
- Publication(s):Almarri et al. 2020
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: 133 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 133 SVs from 25 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5945032 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000019.10 | Chr19 | 38,630,224 | 38,630,274 | ||
nsv5945032 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 39,120,864 | 39,120,914 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17401598 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17401598 | Submitted genomic | NC_000019.10:g.386 30224_38630274del | GRCh38 (hg38) | NC_000019.10 | Chr19 | 38,630,224 | 38,630,274 | ||
nssv17401598 | Remapped | Perfect | NC_000019.9:g.3912 0864_39120914del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 39,120,864 | 39,120,914 |