esv2422433
- Organism: Homo sapiens
- Study:estd196 (Simon-Sanchez et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:141,977
- Publication(s):Simon-Sanchez et al. 2006
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: 559 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 559 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 40 SVs from 7 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 |
---|---|---|---|---|---|---|---|---|---|
esv2422433 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 101,974,547 | 102,116,523 |
esv2422433 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 104,736,829 | 104,878,805 |
esv2422433 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000009.9 | Chr9 | 101,816,384 | 101,958,360 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv5161477 | deletion | ND04275 | SNP array | SNP genotyping analysis | essv5161501, essv5161286 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv5161477 | Remapped | Perfect | NC_000009.12:g.(?_ 101974547)_(102116 523_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 101,974,547 | 102,116,523 |
essv5161477 | Remapped | Perfect | NC_000009.11:g.(?_ 104736829)_(104878 805_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 104,736,829 | 104,878,805 |
essv5161477 | Submitted genomic | NC_000009.9:g.(?_1 01816384)_(1019583 60_?)del | NCBI35 (hg17) | NC_000009.9 | Chr9 | 101,816,384 | 101,958,360 |