nsv959910
- 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:39,411
- 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: 203 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 203 SVs from 38 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959910 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 47,083,718 | 47,123,128 |
| nsv959910 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 47,125,208 | 47,164,618 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021561 | deletion | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021561 | Remapped | Perfect | NC_000003.12:g.(47 067120_47083718)_( 47123128_47235511) del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 47,067,120 | 47,083,718 | 47,123,128 | 47,235,511 |
| nssv3021561 | Submitted genomic | NC_000003.11:g.(47 108610_47125208)_( 47164618_47277001) del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 47,108,610 | 47,125,208 | 47,164,618 | 47,277,001 |