esv993090
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:28,545
- Publication(s):Pang et al. 2010
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: 690 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 693 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 291 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|
esv993090 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 169,251,620 | 169,280,164 |
esv993090 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 169,220,858 | 169,249,402 |
esv993090 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 167,487,482 | 167,516,026 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv3564771 | Remapped | Perfect | NC_000001.11:g.(16 9251620_?)_(?_1692 80164)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 169,251,620 | 169,280,164 |
essv3564771 | Remapped | Perfect | NC_000001.10:g.(16 9220858_?)_(?_1692 49402)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 169,220,858 | 169,249,402 |
essv3564771 | Submitted genomic | NC_000001.9:g.(167 487482_?)_(?_16751 6026)del22556 | NCBI36 (hg18) | NC_000001.9 | Chr1 | 167,487,482 | 167,516,026 |