esv2835
- Organism: Homo sapiens
- Study:estd3 (Wang et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:170
- Publication(s):Wang et al. 2008
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: 334 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 334 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 216 SVs from 14 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
esv2835 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 45,797,532 | 45,797,701 |
esv2835 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 47,217,446 | 47,217,615 |
esv2835 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 46,041,874 | 46,042,043 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv25276 | complex substitution | YH | Sequencing | Read depth and paired-end mapping | 2,682 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|
essv25276 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 45,797,532 | 45,797,701 |
essv25276 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 47,217,446 | 47,217,615 |
essv25276 | Submitted genomic | NCBI36 (hg18) | NC_000021.7 | Chr21 | 46,041,874 | 46,042,043 |