esv3673392
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:sequence alteration
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,638
- Publication(s):Besenbacher et al. 2015
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: 223 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 47 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 183 SVs from 35 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3673392 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | Second Pass | NC_000015.10 | Chr15 | 82,400,087 | 82,402,724 |
| esv3673392 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | First Pass | NT_187606.1 | Chr15|NT_1 87606.1 | 189,178 | 191,815 |
| esv3673392 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 83,068,823 | 83,071,460 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16495257 | sequence alteration | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| essv16495257 | Remapped | Perfect | GRCh38.p12 | First Pass | NT_187606.1 | Chr15|NT_1 87606.1 | 189,178 | 191,815 |
| essv16495257 | Remapped | Perfect | GRCh38.p12 | Second Pass | NC_000015.10 | Chr15 | 82,400,087 | 82,402,724 |
| essv16495257 | Submitted genomic | GRCh37 (hg19) | NC_000015.9 | Chr15 | 83,068,823 | 83,071,460 |