nsv6111238
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:67,662
- Publication(s):Wu 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: 526 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 526 SVs from 73 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6111238 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 150,137,747 | 150,205,408 | ||
nsv6111238 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 149,834,836 | 149,902,497 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17570257 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17570257 | Submitted genomic | NC_000007.14:g.150 137747_150205408in v | GRCh38 (hg38) | NC_000007.14 | Chr7 | 150,137,747 | 150,205,408 | ||
nssv17570257 | Remapped | Perfect | NC_000007.13:g.149 834836_149902497in v | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 149,834,836 | 149,902,497 |