esv3693027
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:77,125
- Publication(s):Palta et al. 2015
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: 379 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 496 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 270 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3693027 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 38,912,275 | 38,989,399 |
| esv3693027 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 38,912,272 | 38,989,396 |
| esv3693027 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 38,902,272 | 38,979,396 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16508711 | Remapped | Perfect | NC_000009.12:g.(?_ 38912275)_(3898939 9_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 38,912,275 | 38,989,399 |
| essv16508711 | Remapped | Perfect | NC_000009.11:g.(?_ 38912272)_(3898939 6_?)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 38,912,272 | 38,989,396 |
| essv16508711 | Submitted genomic | NC_000009.10:g.(?_ 38902272)_(3897939 6_?)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 38,902,272 | 38,979,396 |