nsv6019101
- 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:349,959
- 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: 1077 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1077 SVs from 81 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6019101 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 123,677,222 | 124,027,180 | ||
nsv6019101 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 123,998,367 | 124,348,325 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17560113 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17560113 | Submitted genomic | NC_000006.12:g.123 677222_124027180du p | GRCh38 (hg38) | NC_000006.12 | Chr6 | 123,677,222 | 124,027,180 | ||
nssv17560113 | Remapped | Perfect | NC_000006.11:g.123 998367_124348325du p | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 123,998,367 | 124,348,325 |