nsv1154233
- Organism: Homo sapiens
- Study:nstd105 (Onozawa et al. 2015)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:245
- Description:Insertion of chrM:184-87
- Publication(s):Onozawa 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: 89 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 20 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv1154233 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 137,311,634 | 137,311,878 |
nsv1154233 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 136,647,323 | 136,647,567 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv4004200 | insertion | NA20850 | Sequencing | Sequence alignment | nssv4004127, nssv4004091 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv4004200 | Remapped | Perfect | NC_000005.10:g.(13 7311634_?)_(?_1373 11878)ins97 | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 137,311,634 | 137,311,878 |
nssv4004200 | Submitted genomic | NC_000005.9:g.(136 647323_?)_(?_13664 7567)ins97 | GRCh37 (hg19) | NC_000005.9 | Chr5 | 136,647,323 | 136,647,567 |