nsv6635065
- Organism: Homo sapiens
- Study:nstd227 (Kikas et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:402,673
- Publication(s):Kikas 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: 4290 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 3912 SVs from 58 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6635065 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 1,015,850 | 1,418,522 |
| nsv6635065 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 976,585 | 1,537,415 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18327901 | duplication | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18327901 | Remapped | Pass | NC_000023.11:g.(10 15850_?)_(?_141852 2)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 1,015,850 | 1,418,522 |
| nssv18327901 | Submitted genomic | NC_000023.10:g.(97 6585_?)_(?_1537415 )dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 976,585 | 1,537,415 |