nsv820358
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:37,021
- Publication(s):Ju et al. 2010
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: 722 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 733 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 255 SVs from 21 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 |
---|---|---|---|---|---|---|---|---|---|
nsv820358 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 152,256,301 | 152,293,321 |
nsv820358 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 151,953,386 | 151,990,406 |
nsv820358 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 151,584,319 | 151,621,339 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1420707 | Remapped | Perfect | NC_000007.14:g.(?_ 152256301)_(152293 321_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 152,256,301 | 152,293,321 |
nssv1420707 | Remapped | Perfect | NC_000007.13:g.(?_ 151953386)_(151990 406_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 151,953,386 | 151,990,406 |
nssv1420707 | Submitted genomic | NC_000007.12:g.(?_ 151584319)_(151621 339_?)dup | NCBI36 (hg18) | NC_000007.12 | Chr7 | 151,584,319 | 151,621,339 |