esv1805160
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:195,370
- Publication(s):Pinto 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: 892 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 892 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 282 SVs from 29 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
esv1805160 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 167,885,682 | 167,887,011 | 168,066,057 | 168,081,051 |
esv1805160 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 168,806,833 | 168,808,162 | 168,987,208 | 169,002,202 |
esv1805160 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 169,043,408 | 169,044,737 | 169,223,783 | 169,238,777 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
essv4422141 | Remapped | Perfect | NC_000004.12:g.(16 7885682_167887011) _(168066057_168081 051)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 167,885,682 | 167,887,011 | 168,066,057 | 168,081,051 |
essv4422141 | Remapped | Perfect | NC_000004.11:g.(16 8806833_168808162) _(168987208_169002 202)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 168,806,833 | 168,808,162 | 168,987,208 | 169,002,202 |
essv4422141 | Submitted genomic | NC_000004.10:g.(16 9043408_169044737) _(169223783_169238 777)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 169,043,408 | 169,044,737 | 169,223,783 | 169,238,777 |