esv29965
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,744
- Publication(s):Levy et al. 2007
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: 504 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 503 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 206 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29965 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 119,903,328 | 119,919,071 |
| esv29965 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 119,037,291 | 119,053,034 |
| esv29965 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 118,921,319 | 118,937,062 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84204 | Remapped | Perfect | NC_000023.11:g.(?_ 119903328)_(119919 071_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 119,903,328 | 119,919,071 |
| essv84204 | Remapped | Perfect | NC_000023.10:g.(?_ 119037291)_(119053 034_?)dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 119,037,291 | 119,053,034 |
| essv84204 | Submitted genomic | NC_000023.9:g.(?_1 18921319)_(1189370 62_?)dup | NCBI36 (hg18) | NC_000023.9 | ChrX | 118,921,319 | 118,937,062 |