nsv5665422
- Organism: Homo sapiens
- Study:nstd207 (Ebert 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:60
- Publication(s):Ebert 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: 429 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 429 SVs from 29 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5665422 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 110,689,456 | 110,689,515 | ||
nsv5665422 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 109,932,684 | 109,932,743 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17164704 | Submitted genomic | NC_000023.11:g.110 689456_110689515de lA | GRCh38 (hg38) | NC_000023.11 | ChrX | 110,689,456 | 110,689,515 | ||
nssv17164704 | Remapped | Perfect | NC_000023.10:g.109 932684_109932743de lA | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 109,932,684 | 109,932,743 |