nsv5914132
- 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:9,780,669
- 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: 24174 SVs from 128 studies. See in: genome view
Overlapping variant regions from other studies: 24175 SVs from 128 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5914132 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 26,936,027 | 36,716,695 | ||
nsv5914132 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 26,975,646 | 36,756,300 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17431581 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17431581 | Submitted genomic | NC_000007.14:g.269 36027_36716695del | GRCh38 (hg38) | NC_000007.14 | Chr7 | 26,936,027 | 36,716,695 | ||
nssv17431581 | Remapped | Perfect | NC_000007.13:g.269 75646_36756300del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 26,975,646 | 36,756,300 |