esv1120438
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,053
- 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: 186 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 62 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1120438 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 85,999,036 | 86,005,088 |
| esv1120438 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 86,708,754 | 86,714,806 |
| esv1120438 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 86,765,473 | 86,771,525 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4159963 | Remapped | Perfect | NC_000006.12:g.859 99036_86005088del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 85,999,036 | 86,005,088 |
| essv4159963 | Remapped | Perfect | NC_000006.11:g.867 08754_86714806del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 86,708,754 | 86,714,806 |
| essv4159963 | Submitted genomic | NC_000006.10:g.867 65473_86771525del | NCBI36 (hg18) | NC_000006.10 | Chr6 | 86,765,473 | 86,771,525 |