esv2862949
- Organism: Homo sapiens
- Study:estd209 (Pang et al. 2014b)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35
- Publication(s):Pang et al. 2014
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: 310 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 316 SVs from 34 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv2862949 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 15,865,377 | 15,865,411 |
esv2862949 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 15,865,375 | 15,865,409 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv7132516 | insertion | HuRef | Sequencing | Split read mapping | 471,817 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv7132516 | Remapped | Perfect | NC_000009.12:g.158 65377_15865411insT CATATTTGTGTGTGTGTG TGTGTGTATGTATGTATA TAA | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 15,865,377 | 15,865,411 |
essv7132516 | Submitted genomic | NC_000009.11:g.158 65375_15865409insT CATATTTGTGTGTGTGTG TGTGTGTATGTATGTATA TAA | GRCh37 (hg19) | NC_000009.11 | Chr9 | 15,865,375 | 15,865,409 |