esv1224644
- 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:6,035
- 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: 139 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 139 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 45 SVs from 13 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1224644 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 152,076,869 | 152,082,903 |
esv1224644 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 151,456,430 | 151,462,464 |
esv1224644 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 151,436,623 | 151,442,657 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4012954 | Remapped | Perfect | NC_000005.10:g.152 076869_152082903de l | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 152,076,869 | 152,082,903 |
essv4012954 | Remapped | Perfect | NC_000005.9:g.1514 56430_151462464del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 151,456,430 | 151,462,464 |
essv4012954 | Submitted genomic | NC_000005.8:g.1514 36623_151442657del | NCBI36 (hg18) | NC_000005.8 | Chr5 | 151,436,623 | 151,442,657 |