nsv4715614
- Organism: Homo sapiens
- Study:nstd195 (Mwapagha et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2
- Publication(s):Mwapagha 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: 1189 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 1189 SVs from 74 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4715614 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 43,154,403 | 43,154,404 |
nsv4715614 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 43,658,555 | 43,658,556 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv16234326 | inversion | M456 | Sequencing | Paired-end mapping | 1 | 4,735 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16234326 | Remapped | Perfect | NC_000019.10:g.431 54403_43154404inv | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 43,154,403 | 43,154,404 |
nssv16234326 | Submitted genomic | NC_000019.9:g.4365 8555_43658556inv | GRCh37 (hg19) | NC_000019.9 | Chr19 | 43,658,555 | 43,658,556 |