nsv6633451
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:13
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,635
- Publication(s):Zarrei et al. 2023
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: 273 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 279 SVs from 53 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6633451 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nsv6633451 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18303469 | deletion | OSC6045 | SNP array | Probe signal intensity | 11 |
| nssv18303582 | deletion | OSC5936 | SNP array | Probe signal intensity | 9 |
| nssv18304246 | deletion | OSC6196 | SNP array | Probe signal intensity | 11 |
| nssv18308596 | deletion | OSC6853 | SNP array | Probe signal intensity | 6 |
| nssv18309516 | deletion | OSC7058 | SNP array | Probe signal intensity | 9 |
| nssv18311309 | deletion | OSC7456 | SNP array | Probe signal intensity | 9 |
| nssv18311632 | deletion | OSC7403 | SNP array | Probe signal intensity | 11 |
| nssv18312984 | deletion | OSC7706 | SNP array | Probe signal intensity | 9 |
| nssv18314092 | deletion | OSC7818 | SNP array | Probe signal intensity | 11 |
| nssv18314256 | deletion | OSC7942 | SNP array | Probe signal intensity | 10 |
| nssv18315225 | deletion | OSC7972 | SNP array | Probe signal intensity | 9 |
| nssv18316400 | deletion | OSC8389 | SNP array | Probe signal intensity | 11 |
| nssv18320430 | deletion | OSC8815 | SNP array | Probe signal intensity | 9 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18303469 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18303582 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18304246 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18308596 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18309516 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18311309 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18311632 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18312984 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18314092 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18314256 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18315225 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18316400 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18320430 | Remapped | Perfect | NC_000009.12:g.(?_ 32105256)_(3212289 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 32,105,256 | 32,122,890 |
| nssv18303469 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18303582 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18304246 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18308596 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18309516 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18311309 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18311632 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18312984 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18314092 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18314256 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18315225 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18316400 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 | ||
| nssv18320430 | Submitted genomic | NC_000009.11:g.(?_ 32105254)_(3212288 8_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 32,105,254 | 32,122,888 |