esv30006
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:22,511
- 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: 846 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 846 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 369 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv30006 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 73,555,361 | 73,577,871 |
| esv30006 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 74,022,065 | 74,044,575 |
| esv30006 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 73,091,818 | 73,114,328 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84245 | Remapped | Perfect | NC_000014.9:g.(?_7 3555361)_(73577871 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 73,555,361 | 73,577,871 |
| essv84245 | Remapped | Perfect | NC_000014.8:g.(?_7 4022065)_(74044575 _?)dup | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 74,022,065 | 74,044,575 |
| essv84245 | Submitted genomic | NC_000014.7:g.(?_7 3091818)_(73114328 _?)dup | NCBI36 (hg18) | NC_000014.7 | Chr14 | 73,091,818 | 73,114,328 |