nsv5906033
- 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:1,028
- 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: 294 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 294 SVs from 43 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5906033 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 16,869,603 | 16,870,630 | ||
nsv5906033 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 16,869,712 | 16,870,739 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17423051 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17423051 | Submitted genomic | NC_000005.10:g.168 69603_16870630del | GRCh38 (hg38) | NC_000005.10 | Chr5 | 16,869,603 | 16,870,630 | ||
nssv17423051 | Remapped | Perfect | NC_000005.9:g.1686 9712_16870739del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 16,869,712 | 16,870,739 |