nsv4431137
- Organism: Homo sapiens
- Study:nstd161 (Nazaryan-Petersen et al. 2019)
- Variant Type:complex chromosomal rearrangement
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Nazaryan-Petersen et al. 2019
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: 196 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 116 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 291 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 116 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 291 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
---|---|---|---|---|---|---|---|---|---|---|
nsv4431137 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 148,636,922 | 148,636,922 | + |
nsv4431137 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 84,057,618 | 84,057,618 | + |
nsv4431137 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 89,357,294 | 89,357,294 | + |
nsv4431137 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 91,455,126 | 91,455,126 | + |
nsv4431137 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 148,334,014 | 148,334,014 | + | ||
nsv4431137 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 83,686,934 | 83,686,934 | + | ||
nsv4431137 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 88,986,608 | 88,986,608 | + | ||
nsv4431137 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 91,084,441 | 91,084,441 | + |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
---|---|---|---|---|---|---|---|---|---|
nssv15745547 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 84,057,618 | 84,057,618 | + |
nssv15745547 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 89,357,294 | 89,357,294 | + |
nssv15745546 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 91,455,126 | 91,455,126 | + |
nssv15745546 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 148,636,922 | 148,636,922 | + |
nssv15745547 | Submitted genomic | GRCh37 (hg19) | NC_000007.13 | Chr7 | 83,686,934 | 83,686,934 | + | ||
nssv15745547 | Submitted genomic | GRCh37 (hg19) | NC_000007.13 | Chr7 | 88,986,608 | 88,986,608 | + | ||
nssv15745546 | Submitted genomic | GRCh37 (hg19) | NC_000007.13 | Chr7 | 91,084,441 | 91,084,441 | + | ||
nssv15745546 | Submitted genomic | GRCh37 (hg19) | NC_000007.13 | Chr7 | 148,334,014 | 148,334,014 | + |