nsv3565902
- Organism: Homo sapiens
- Study:nstd152 (Chaisson et al. 2019)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:5
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Insertion of a Alu mobile element relative to the reference
- Publication(s):Chaisson 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: 445 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 449 SVs from 48 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3565902 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) | ||
nsv3565902 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Zygosity | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv14344523 | alu insertion | SAMN00006466 | Sequencing | Sequence alignment | Heterozygous | 14,137 |
nssv14344524 | alu insertion | SAMN00006579 | Sequencing | Sequence alignment | Heterozygous | 13,953 |
nssv14344525 | alu insertion | SAMN00006580 | Sequencing | Sequence alignment | Heterozygous | 14,212 |
nssv14344526 | alu insertion | SAMN00006581 | Sequencing | Sequence alignment | Heterozygous | 41,185 |
nssv14344527 | alu insertion | SAMN00001694 | Sequencing | Sequence alignment | Heterozygous | 16,419 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14344523 | Submitted genomic | NC_000009.12:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) | ||
nssv14344524 | Submitted genomic | NC_000009.12:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) | ||
nssv14344525 | Submitted genomic | NC_000009.12:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) | ||
nssv14344526 | Submitted genomic | NC_000009.12:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) | ||
nssv14344527 | Submitted genomic | NC_000009.12:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) | ||
nssv14344523 | Remapped | Perfect | NC_000009.11:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) |
nssv14344524 | Remapped | Perfect | NC_000009.11:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) |
nssv14344525 | Remapped | Perfect | NC_000009.11:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) |
nssv14344526 | Remapped | Perfect | NC_000009.11:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) |
nssv14344527 | Remapped | Perfect | NC_000009.11:g.(70 35312_7035342)_(70 35312_7035342)ins2 80 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 7,035,327 (-15, +15) | 7,035,327 (-15, +15) |