nsv499089
- Organism: Homo sapiens
- Study:nstd47 (Kidd et al. 2010b)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,368
- Publication(s):Kidd et al. 2010
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: 113 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 110 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 26 SVs from 12 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv499089 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 50,887,229 | 50,897,596 |
nsv499089 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 50,925,339 | 50,935,706 |
nsv499089 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 50,899,679 | 50,910,048 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv585538 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv585538 | Remapped | Good | NC_000003.12:g.508 87229_50897596inv | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 50,887,229 | 50,897,596 |
nssv585538 | Remapped | Good | NC_000003.11:g.509 25339_50935706inv | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 50,925,339 | 50,935,706 |
nssv585538 | Submitted genomic | NC_000003.10:g.508 99679_50910048inv | NCBI36 (hg18) | NC_000003.10 | Chr3 | 50,899,679 | 50,910,048 |