nsv6019943
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:293,761
- 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: 2330 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 2868 SVs from 88 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6019943 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 60,309,164 | 60,602,924 | ||
| nsv6019943 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 57,301,494 | 57,570,671 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17567181 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17567181 | Submitted genomic | NC_000006.12:g.603 09164_60602924del | GRCh38 (hg38) | NC_000006.12 | Chr6 | 60,309,164 | 60,602,924 | ||
| nssv17567181 | Remapped | Pass | NC_000006.11:g.573 01494_57570671del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 57,301,494 | 57,570,671 |