esv274910
- Organism: Homo sapiens
- Study:estd176 (Banerjee et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,960
- Publication(s):Banerjee et al. 2011
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: 162 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 162 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 48 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv274910 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 97,317,057 | 97,317,178 | 97,317,387 | 97,339,016 |
| esv274910 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 96,946,369 | 96,946,490 | 96,946,699 | 96,968,328 |
| esv274910 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 96,784,305 | 96,784,426 | 96,784,635 | 96,806,264 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv2585532 | copy number loss | SNP array | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv2585532 | Remapped | Perfect | NC_000007.14:g.(97 317057_97317178)_( 97317387_97339016) del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 97,317,057 | 97,317,178 | 97,317,387 | 97,339,016 |
| essv2585532 | Remapped | Perfect | NC_000007.13:g.(96 946369_96946490)_( 96946699_96968328) del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 96,946,369 | 96,946,490 | 96,946,699 | 96,968,328 |
| essv2585532 | Submitted genomic | NC_000007.12:g.(96 784305_96784426)_( 96784635_96806264) del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 96,784,305 | 96,784,426 | 96,784,635 | 96,806,264 |