nsv4385226
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:34
- Validation:Not tested
- Clinical Assertions: No
- Region Size:295,646
- Publication(s):Zarrei et al. 2019
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: 1635 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 1504 SVs from 93 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4385226 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nsv4385226 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15616199 | copy number gain | 1-0792-003 | SNP array | Genotyping | 15 |
| nssv15617728 | copy number gain | 1-0838-003 | SNP array | Genotyping | 27 |
| nssv15622802 | copy number gain | 1-0224-001 | SNP array | Genotyping | 29 |
| nssv15624699 | copy number gain | 1-0332-002 | SNP array | Genotyping | 28 |
| nssv15637385 | copy number gain | 13-0094-004 | SNP array | Genotyping | 24 |
| nssv15638664 | copy number gain | 14-0010-001 | SNP array | Genotyping | 14 |
| nssv15640406 | copy number gain | 14-0152-004 | SNP array | Genotyping | 19 |
| nssv15641444 | copy number gain | 14-0351-001 | SNP array | Genotyping | 11 |
| nssv15643722 | copy number gain | 2-0122-003 | SNP array | Genotyping | 16 |
| nssv15644979 | copy number gain | 2-0270-004 | SNP array | Genotyping | 13 |
| nssv15651682 | copy number gain | 2-1528-003 | SNP array | Genotyping | 16 |
| nssv15652560 | copy number gain | 2-1561-003 | SNP array | Genotyping | 18 |
| nssv15653425 | copy number gain | 2-1559-003 | SNP array | Genotyping | 21 |
| nssv15657620 | copy number gain | 4-0039-002 | SNP array | Genotyping | 25 |
| nssv15658669 | copy number gain | 3-0544-000 | SNP array | Genotyping | 17 |
| nssv15658725 | copy number gain | 3-0602-000 | SNP array | Genotyping | 28 |
| nssv15659960 | copy number gain | 5-0003-001 | SNP array | Genotyping | 27 |
| nssv15664639 | copy number gain | 4-0078-002 | SNP array | Genotyping | 34 |
| nssv15666064 | copy number gain | 5-0037-003 | SNP array | Genotyping | 18 |
| nssv15670139 | copy number gain | 7-0258-004 | SNP array | Genotyping | 30 |
| nssv15671276 | copy number gain | 7-0280-003 | SNP array | Genotyping | 21 |
| nssv15672557 | copy number gain | 9-0009-003 | SNP array | Genotyping | 19 |
| nssv15673739 | copy number gain | 227576 | SNP array | Genotyping | 15 |
| nssv15676141 | copy number gain | 206764 | SNP array | Genotyping | 16 |
| nssv15676484 | copy number gain | 233006S | SNP array | Genotyping | 21 |
| nssv15677004 | copy number gain | 215805 | SNP array | Genotyping | 21 |
| nssv15677645 | copy number gain | 218118 | SNP array | Genotyping | 29 |
| nssv15685628 | copy number gain | OCD168-8961233 | SNP array | Genotyping | 19 |
| nssv15686738 | copy number gain | OCD24-S_896443 | SNP array | Genotyping | 16 |
| nssv15686777 | copy number gain | OCD26-S_896513 | SNP array | Genotyping | 28 |
| nssv15690312 | copy number gain | OCD141-0625-7921-2 | SNP array | Genotyping | 26 |
| nssv15698732 | copy number gain | 243953S | SNP array | Genotyping | 21 |
| nssv15699996 | copy number gain | 169623 | SNP array | Genotyping | 20 |
| nssv15700670 | copy number gain | 197703 | SNP array | Genotyping | 17 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15616199 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15617728 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15622802 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15624699 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15637385 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15638664 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15640406 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15641444 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15643722 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15644979 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15651682 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15652560 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15653425 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15657620 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15658669 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15658725 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15659960 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15664639 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15666064 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15670139 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15671276 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15672557 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15673739 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15676141 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15676484 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15677004 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15677645 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15685628 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15686738 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15686777 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15690312 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15698732 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15699996 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15700670 | Remapped | Perfect | NC_000016.10:g.(?_ 35225812)_(3552145 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,225,812 | 35,521,457 |
| nssv15616199 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15617728 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15622802 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15624699 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15637385 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15638664 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15640406 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15641444 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15643722 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15644979 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15651682 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15652560 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15653425 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15657620 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15658669 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15658725 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15659960 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15664639 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15666064 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15670139 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15671276 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15672557 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15673739 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15676141 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15676484 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15677004 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15677645 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15685628 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15686738 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15686777 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15690312 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15698732 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15699996 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 | ||
| nssv15700670 | Submitted genomic | NC_000016.9:g.(?_3 4460183)_(34755828 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,460,183 | 34,755,828 |