nsv6027019
- 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:226,013
- 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: 1340 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 1340 SVs from 80 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6027019 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000018.10 | Chr18 | 66,423,478 | 66,649,490 | ||
nsv6027019 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 64,090,715 | 64,316,727 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17623782 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17623782 | Submitted genomic | NC_000018.10:g.664 23478_66649490dup | GRCh38 (hg38) | NC_000018.10 | Chr18 | 66,423,478 | 66,649,490 | ||
nssv17623782 | Remapped | Perfect | NC_000018.9:g.6409 0715_64316727dup | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 64,090,715 | 64,316,727 |