nsv972230
- Organism: Homo sapiens
- Study:nstd82 (Sudmant et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:76,958
- Publication(s):Sudmant et al. 2013
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: 1728 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1728 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1101 SVs from 33 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv972230 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 39,368,872 | 39,445,829 |
nsv972230 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 39,226,391 | 39,303,348 |
nsv972230 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 39,345,548 | 39,422,505 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv2758502 | Remapped | Perfect | NC_000008.11:g.(?_ 39368872)_(3944582 9_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 39,368,872 | 39,445,829 |
nssv2759585 | Remapped | Perfect | NC_000008.11:g.(?_ 39368872)_(3944582 9_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 39,368,872 | 39,445,829 |
nssv2759742 | Remapped | Perfect | NC_000008.11:g.(?_ 39368872)_(3944582 9_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 39,368,872 | 39,445,829 |
nssv2758502 | Remapped | Perfect | NC_000008.10:g.(?_ 39226391)_(3930334 8_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 39,226,391 | 39,303,348 |
nssv2759585 | Remapped | Perfect | NC_000008.10:g.(?_ 39226391)_(3930334 8_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 39,226,391 | 39,303,348 |
nssv2759742 | Remapped | Perfect | NC_000008.10:g.(?_ 39226391)_(3930334 8_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 39,226,391 | 39,303,348 |
nssv2758502 | Submitted genomic | NC_000008.9:g.(?_3 9345548)_(39422505 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 39,345,548 | 39,422,505 | ||
nssv2759585 | Submitted genomic | NC_000008.9:g.(?_3 9345548)_(39422505 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 39,345,548 | 39,422,505 | ||
nssv2759742 | Submitted genomic | NC_000008.9:g.(?_3 9345548)_(39422505 _?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 39,345,548 | 39,422,505 |