esv3671461
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:novel sequence insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- 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: 271 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 271 SVs from 50 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3671461 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 150,953,968 | 150,953,968 |
esv3671461 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 151,875,120 | 151,875,120 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
essv16493518 | novel sequence insertion | Sequencing | de novo sequence assembly |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv16493518 | Remapped | Perfect | NC_000004.12:g.150 953968_150953969in s80 | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 150,953,968 | 150,953,968 |
essv16493518 | Submitted genomic | NC_000004.11:g.151 875120_151875121in s80 | GRCh37 (hg19) | NC_000004.11 | Chr4 | 151,875,120 | 151,875,120 |