nsv6633561
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:95,255
- Publication(s):Zarrei et al. 2023
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: 572 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 574 SVs from 55 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6633561 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 103,945,722 | 104,040,976 |
| nsv6633561 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 103,200,296 | 103,295,543 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18293333 | Remapped | Good | NC_000023.11:g.(?_ 103945722)_(104040 976_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 103,945,722 | 104,040,976 |
| nssv18325310 | Remapped | Good | NC_000023.11:g.(?_ 103945722)_(104040 976_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 103,945,722 | 104,040,976 |
| nssv18293333 | Submitted genomic | NC_000023.10:g.(?_ 103200296)_(103295 543_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 103,200,296 | 103,295,543 | ||
| nssv18325310 | Submitted genomic | NC_000023.10:g.(?_ 103200296)_(103295 543_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 103,200,296 | 103,295,543 |