nsv4388329
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:109,873
- Publication(s):Zarrei et al. 2019
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: 481 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 481 SVs from 40 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4388329 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 120,876,046 | 120,985,918 |
| nsv4388329 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 120,009,900 | 120,119,772 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15629744 | Remapped | Perfect | NC_000023.11:g.(?_ 120876046)_(120985 918_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 120,876,046 | 120,985,918 |
| nssv15649175 | Remapped | Perfect | NC_000023.11:g.(?_ 120876046)_(120985 918_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 120,876,046 | 120,985,918 |
| nssv15629744 | Submitted genomic | NC_000023.10:g.(?_ 120009900)_(120119 772_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 120,009,900 | 120,119,772 | ||
| nssv15649175 | Submitted genomic | NC_000023.10:g.(?_ 120009900)_(120119 772_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 120,009,900 | 120,119,772 |