esv2632239
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:originalFile=Yoruban_small_indel.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:Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv2632239 | Remapped | Perfect | GRCh38.p12 | non-nuclear | First Pass | NC_012920.1 | ChrMT | 2,709 | 2,709 |
esv2632239 | Remapped | Perfect | GRCh37.p13 | non-nuclear | First Pass | NC_012920.1 | ChrMT | 2,709 | 2,709 |
esv2632239 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_001807.4 | ChrMT | 2,711 | 2,711 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv5262603 | Remapped | Perfect | NC_012920.1:g.2709 _2710ins? | GRCh38.p12 | First Pass | NC_012920.1 | ChrMT | 2,709 | 2,709 |
essv5262603 | Remapped | Perfect | NC_012920.1:g.2709 _2710ins? | GRCh37.p13 | First Pass | NC_012920.1 | ChrMT | 2,709 | 2,709 |
essv5262603 | Submitted genomic | NC_001807.4:g.2711 _2712ins? | NCBI36 (hg18) | NC_001807.4 | ChrMT | 2,711 | 2,711 |