nsv5712735
- Organism: Homo sapiens
- Study:nstd211 (Chuang et al. 2021)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Insertion of a HERV mobile element relative to the reference
- Publication(s):Chuang et al. 2021
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: 94 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5712735 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 25,588,105 | 25,588,105 | ||
nsv5712735 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 25,914,596 | 25,914,596 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17214482 | herv insertion | Sequencing | Other |
nssv17232609 | herv insertion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17214482 | Submitted genomic | NC_000001.11:g.255 88105_25588106ins8 656 | GRCh38 (hg38) | NC_000001.11 | Chr1 | 25,588,105 | 25,588,105 | ||
nssv17232609 | Submitted genomic | NC_000001.11:g.255 88105_25588106ins6 38 | GRCh38 (hg38) | NC_000001.11 | Chr1 | 25,588,105 | 25,588,105 | ||
nssv17214482 | Remapped | Perfect | NC_000001.10:g.259 14596_25914597ins8 656 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 25,914,596 | 25,914,596 |
nssv17232609 | Remapped | Perfect | NC_000001.10:g.259 14596_25914597ins6 38 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 25,914,596 | 25,914,596 |