esv2513521
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,338
- Description:originalFile=Yoruban_inv.gff
- Publication(s):McKernan et al. 2009
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: 145 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 145 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 47 SVs from 11 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
esv2513521 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 84,520,793 | 84,521,131 | 84,522,003 | 84,522,130 |
esv2513521 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 87,135,708 | 87,136,046 | 87,136,918 | 87,137,045 |
esv2513521 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 86,325,528 | 86,325,866 | 86,326,738 | 86,326,865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv5389558 | Remapped | Perfect | NC_000009.12:g.(84 520793_84521131)_( 84522003_84522130) inv | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 84,520,793 | 84,521,131 | 84,522,003 | 84,522,130 |
essv5389558 | Remapped | Perfect | NC_000009.11:g.(87 135708_87136046)_( 87136918_87137045) inv | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 87,135,708 | 87,136,046 | 87,136,918 | 87,137,045 |
essv5389558 | Submitted genomic | NC_000009.10:g.(86 325528_86325866)_( 86326738_86326865) inv | NCBI36 (hg18) | NC_000009.10 | Chr9 | 86,325,528 | 86,325,866 | 86,326,738 | 86,326,865 |