nsv474990
- Organism: Homo sapiens
- Study:nstd35 (Kidd et al. 2010)
- Variant Type:complex substitution
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:85
- Description:complex allele - no allele length provided
- Publication(s):Kidd 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: 99 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 15 SVs from 11 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv474990 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 49,489,776 | 49,489,860 |
nsv474990 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 48,559,526 | 48,559,610 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv3019885 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 49,489,776 | 49,489,860 |
nssv3019885 | Submitted genomic | NCBI36 (hg18) | NC_000014.7 | Chr14 | 48,559,526 | 48,559,610 |