nsv4380030
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:42
- Validation:Not tested
- Clinical Assertions: No
- Region Size:27,394
- 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: 942 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 943 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4380030 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nsv4380030 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15613790 | copy number gain | 1-0707-001 | SNP array | Genotyping | 20 |
| nssv15615590 | copy number gain | 1-0798-003 | SNP array | Genotyping | 17 |
| nssv15617041 | copy number gain | 1-0158-003 | SNP array | Genotyping | 18 |
| nssv15617155 | copy number gain | 1-0777-003 | SNP array | Genotyping | 26 |
| nssv15618060 | copy number gain | 1-0882-003 | SNP array | Genotyping | 27 |
| nssv15618528 | copy number gain | 1-0901-004 | SNP array | Genotyping | 19 |
| nssv15619112 | copy number gain | 1-0926-003 | SNP array | Genotyping | 20 |
| nssv15620591 | copy number gain | 1-0951-003 | SNP array | Genotyping | 25 |
| nssv15623107 | copy number gain | 1-1054-003 | SNP array | Genotyping | 19 |
| nssv15623908 | copy number gain | 1-0043-003 | SNP array | Genotyping | 27 |
| nssv15636765 | copy number gain | 13-0150-002 | SNP array | Genotyping | 21 |
| nssv15640075 | copy number gain | 14-0103-002 | SNP array | Genotyping | 23 |
| nssv15645547 | copy number gain | 2-0305-001 | SNP array | Genotyping | 20 |
| nssv15646245 | copy number gain | 2-0003-002 | SNP array | Genotyping | 23 |
| nssv15650673 | copy number gain | 2-1362-002 | SNP array | Genotyping | 16 |
| nssv15651112 | copy number gain | 2-1415-005 | SNP array | Genotyping | 14 |
| nssv15654793 | copy number loss | 3-0289-000 | SNP array | Genotyping | 25 |
| nssv15661128 | copy number gain | 4-0079-003 | SNP array | Genotyping | 18 |
| nssv15666106 | copy number gain | 5-0084-002 | SNP array | Genotyping | 18 |
| nssv15666214 | copy number gain | 5-0087-003 | SNP array | Genotyping | 20 |
| nssv15669532 | copy number gain | 7-0265-003 | SNP array | Genotyping | 20 |
| nssv15669827 | copy number gain | 7-0251-003 | SNP array | Genotyping | 21 |
| nssv15670369 | copy number gain | 7-0297-003 | SNP array | Genotyping | 24 |
| nssv15670940 | copy number gain | 7-0286-004 | SNP array | Genotyping | 32 |
| nssv15672022 | copy number gain | 7-0319-003 | SNP array | Genotyping | 23 |
| nssv15672470 | copy number gain | 9-0006-003 | SNP array | Genotyping | 19 |
| nssv15673147 | copy number loss | 9-0028-003 | SNP array | Genotyping | 16 |
| nssv15674286 | copy number gain | 9-0033-002 | SNP array | Genotyping | 22 |
| nssv15674447 | copy number gain | 9-0036-001 | SNP array | Genotyping | 24 |
| nssv15675972 | copy number gain | 216579 | SNP array | Genotyping | 25 |
| nssv15676999 | copy number gain | 215805 | SNP array | Genotyping | 21 |
| nssv15677101 | copy number gain | 218105 | SNP array | Genotyping | 20 |
| nssv15678129 | copy number gain | 245251S | SNP array | Genotyping | 22 |
| nssv15679860 | copy number gain | 211146 | SNP array | Genotyping | 24 |
| nssv15680757 | copy number gain | 216161 | SNP array | Genotyping | 22 |
| nssv15680829 | copy number gain | 232720S | SNP array | Genotyping | 18 |
| nssv15695620 | copy number gain | 217438 | SNP array | Genotyping | 25 |
| nssv15700758 | copy number gain | 162445 | SNP array | Genotyping | 17 |
| nssv15701030 | copy number gain | 187962 | SNP array | Genotyping | 25 |
| nssv15701231 | copy number gain | 183057 | SNP array | Genotyping | 24 |
| nssv15702166 | copy number gain | 154659 | SNP array | Genotyping | 21 |
| nssv15702534 | copy number gain | 199593 | SNP array | Genotyping | 20 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15613790 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15615590 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15617041 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15617155 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15618060 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15618528 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15619112 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15620591 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15623107 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15623908 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15636765 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15640075 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15645547 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15646245 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15650673 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15651112 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15654793 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15661128 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15666106 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15666214 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15669532 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15669827 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15670369 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15670940 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15672022 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15672470 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15673147 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15674286 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15674447 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15675972 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15676999 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15677101 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15678129 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15679860 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15680757 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15680829 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15695620 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15700758 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15701030 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15701231 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15702166 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15702534 | Remapped | Perfect | NC_000012.12:g.(?_ 11067396)_(1109478 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,067,396 | 11,094,789 |
| nssv15613790 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15615590 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15617041 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15617155 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15618060 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15618528 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15619112 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15620591 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15623107 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15623908 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15636765 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15640075 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15645547 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15646245 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15650673 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15651112 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15654793 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)del | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15661128 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15666106 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15666214 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15669532 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15669827 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15670369 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15670940 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15672022 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15672470 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15673147 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)del | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15674286 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15674447 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15675972 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15676999 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15677101 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15678129 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15679860 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15680757 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15680829 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15695620 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15700758 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15701030 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15701231 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15702166 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 | ||
| nssv15702534 | Submitted genomic | NC_000012.11:g.(?_ 11219995)_(1124738 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 11,219,995 | 11,247,388 |