nsv6112646
- 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:50,338
- 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: 409 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 409 SVs from 63 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6112646 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 195,154,852 | 195,205,189 | ||
nsv6112646 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 196,019,576 | 196,069,913 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17528753 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17528753 | Submitted genomic | NC_000002.12:g.195 154852_195205189in v | GRCh38 (hg38) | NC_000002.12 | Chr2 | 195,154,852 | 195,205,189 | ||
nssv17528753 | Remapped | Perfect | NC_000002.11:g.196 019576_196069913in v | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 196,019,576 | 196,069,913 |