nsv959161
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:101,404
- Publication(s):Poultney 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: 318 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 318 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv959161 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 98,093,091 | 98,194,494 |
| nsv959161 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 98,709,554 | 98,810,957 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021465 | duplication | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021465 | Remapped | Perfect | NC_000002.12:g.(97 927487_98093091)_( 98194494_98211928) dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,927,487 | 98,093,091 | 98,194,494 | 98,211,928 |
| nssv3021465 | Submitted genomic | NC_000002.11:g.(98 543950_98709554)_( 98810957_98828391) dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,543,950 | 98,709,554 | 98,810,957 | 98,828,391 |