esv1007074
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:20,777
- Publication(s):Pang et al. 2010
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: 216 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 216 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 53 SVs from 14 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
esv1007074 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 197,778,907 | 197,799,683 |
esv1007074 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 197,748,037 | 197,768,813 |
esv1007074 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 196,014,660 | 196,035,436 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv3563607 | Remapped | Perfect | NC_000001.11:g.(19 7778907_?)_(?_1977 99683)inv20777 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 197,778,907 | 197,799,683 |
essv3563607 | Remapped | Perfect | NC_000001.10:g.(19 7748037_?)_(?_1977 68813)inv20777 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 197,748,037 | 197,768,813 |
essv3563607 | Submitted genomic | NC_000001.9:g.(196 014660_?)_(?_19603 5436)inv20777 | NCBI36 (hg18) | NC_000001.9 | Chr1 | 196,014,660 | 196,035,436 |