nsv959803
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:86,831
- 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: 512 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 512 SVs from 85 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959803 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 160,548,476 | 160,635,306 |
| nsv959803 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 160,969,508 | 161,056,338 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021647 | duplication | Sequencing | Read depth |
| nssv3021568 | duplication | Sequencing | Read depth |
| nssv3021832 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021647 | Remapped | Perfect | NC_000006.12:g.(16 0547939_160548476) _(160594119_160595 352)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,547,939 | 160,548,476 | 160,594,119 | 160,595,352 |
| nssv3021568 | Remapped | Perfect | NC_000006.12:g.(16 0547939_160548476) _(160601100_160606 475)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,547,939 | 160,548,476 | 160,601,100 | 160,606,475 |
| nssv3021832 | Remapped | Perfect | NC_000006.12:g.(16 0547939_160548476) _(160635306_160702 303)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,547,939 | 160,548,476 | 160,635,306 | 160,702,303 |
| nssv3021647 | Submitted genomic | NC_000006.11:g.(16 0968971_160969508) _(161015151_161016 384)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 160,968,971 | 160,969,508 | 161,015,151 | 161,016,384 | ||
| nssv3021568 | Submitted genomic | NC_000006.11:g.(16 0968971_160969508) _(161022132_161027 507)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 160,968,971 | 160,969,508 | 161,022,132 | 161,027,507 | ||
| nssv3021832 | Submitted genomic | NC_000006.11:g.(16 0968971_160969508) _(161056338_161123 335)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 160,968,971 | 160,969,508 | 161,056,338 | 161,123,335 |