esv1182290
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:5,449
- 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: 187 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 187 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 70 SVs from 20 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1182290 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 22,050,869 | 22,056,317 |
esv1182290 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 22,092,361 | 22,097,809 |
esv1182290 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 22,067,365 | 22,072,813 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4069795 | Remapped | Perfect | NC_000003.12:g.220 50869_22056317del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 22,050,869 | 22,056,317 |
essv4069795 | Remapped | Perfect | NC_000003.11:g.220 92361_22097809del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 22,092,361 | 22,097,809 |
essv4069795 | Submitted genomic | NC_000003.10:g.220 67365_22072813del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 22,067,365 | 22,072,813 |