nsv479545
- Organism: Homo sapiens
- Study:nstd35 (Kidd et al. 2010)
- Variant Type:novel sequence insertion
- Method Type:Sequencing
- Variant is Defined by:GU267048
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,272
- Description:This variant by definition has no placement. It represents a contig assembled from multiple read pairs, no part of which could be mapped to assembly NCBI35.
- Publication(s):Kidd et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nsv479545 | Remapped | Good | GRCh38.p12 | Primary Assembly | NT_005403.18 | Chr2|NT_00 5403.18 | 144,403,721 | 144,404,992 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3014752 | novel sequence insertion | Sequencing | One end anchored assembly |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv3014752 | Remapped | Good | NT_005403.18:g.144 403721_144404992in s? | GRCh38.p12 | NT_005403.18 | Chr2|NT_00 5403.18 | 144,403,721 | 144,404,992 |