esv33779
- Organism: Homo sapiens
- Study:estd24 (de Smith et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,375
- Publication(s):de Smith 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: 336 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 336 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 11 SVs from 6 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
esv33779 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 197,647,013 | 197,660,387 |
esv33779 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 197,373,884 | 197,387,258 |
esv33779 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000003.9 | Chr3 | 198,862,194 | 198,875,568 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv96648 | Remapped | Perfect | NC_000003.12:g.(19 7612428_197647013) _(197660387_197667 616)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 197,612,428 | 197,647,013 | 197,660,387 | 197,667,616 |
essv99896 | Remapped | Perfect | NC_000003.12:g.(19 7657848_197658517) _(197659895_197660 357)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 197,657,848 | 197,658,517 | 197,659,895 | 197,660,357 |
essv96648 | Remapped | Perfect | NC_000003.11:g.(19 7339299_197373884) _(197387258_197394 487)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 197,339,299 | 197,373,884 | 197,387,258 | 197,394,487 |
essv99896 | Remapped | Perfect | NC_000003.11:g.(19 7384719_197385388) _(197386766_197387 228)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 197,384,719 | 197,385,388 | 197,386,766 | 197,387,228 |
essv96648 | Submitted genomic | NC_000003.9:g.(198 827609_198862194)_ (198875568_1988827 97)del | NCBI35 (hg17) | NC_000003.9 | Chr3 | 198,827,609 | 198,862,194 | 198,875,568 | 198,882,797 | ||
essv99896 | Submitted genomic | NC_000003.9:g.(198 873029_198873698)_ (198875076_1988755 38)dup | NCBI35 (hg17) | NC_000003.9 | Chr3 | 198,873,029 | 198,873,698 | 198,875,076 | 198,875,538 |