nsv4426795
- Organism: Homo sapiens
- Study:nstd174 (DGV Gold Standard)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:283,056
- DGV: gssvL19604
- dbVar: essv14198459
- dbVar: essv14198460
- dbVar: essv14198461
- dbVar: essv14198462
- dbVar: essv14198463
- dbVar: essv14198464
- dbVar: essv14198465
- dbVar: essv14198466
- dbVar: essv14198467
- dbVar: essv14198468
- dbVar: essv14198469
- dbVar: essv14198470
- dbVar: essv14198471
- dbVar: essv14198472
- dbVar: essv14198473
- dbVar: essv14198474
- dbVar: essv14198475
- dbVar: essv14198476
- dbVar: essv14198477
- dbVar: essv14198478
- dbVar: essv14198479
- dbVar: essv14198480
- dbVar: essv14198481
- dbVar: essv14198482
- dbVar: essv14198483
- dbVar: essv14198484
- dbVar: essv14198485
- dbVar: essv14198486
- dbVar: essv14198487
- dbVar: essv14198488
- dbVar: essv14198489
- dbVar: essv14198490
- dbVar: essv14198491
- dbVar: essv14198492
- dbVar: essv14198493
- dbVar: essv14198494
- dbVar: essv14198495
- dbVar: essv14198496
- dbVar: essv14198497
- dbVar: essv5404409
- dbVar: essv5571510
- dbVar: essv5786400
- dbVar: essv6110888
- dbVar: essv6688195
- dbVar: essv6716681
- dbVar: essv6740964
- dbVar: essv6749594
- dbVar: essv6752489
- dbVar: essv6755452
- dbVar: essv6827597
- dbVar: essv6891170
- dbVar: essv6900557
- dbVar: essv6907884
- dbVar: essv6907895
- dbVar: essv6959091
- dbVar: essv6996093
- dbVar: nssv3504316
- dbVar: nssv3504889
- dbVar: nssv3507607
- dbVar: nssv3508675
- dbVar: nssv3508805
- dbVar: nssv3511277
- dbVar: nssv3515047
- dbVar: nssv3516341
- dbVar: nssv3518552
- dbVar: nssv3518896
- dbVar: nssv3519635
- dbVar: nssv3710624
- Overlapping Genes
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: 1023 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1019 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 | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4426795 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 67,706,963 | 67,733,879 | 67,971,501 | 67,990,018 |
nsv4426795 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 67,474,434 | 67,501,350 | 67,738,972 | 67,757,489 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15718135 | copy number loss | Multiple | Multiple |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15718135 | Remapped | Perfect | NC_000011.10:g.(67 706963_67733879)_( 67971501_67990018) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,706,963 | 67,733,879 | 67,971,501 | 67,990,018 |
nssv15718135 | Submitted genomic | NC_000011.9:g.(674 74434_67501350)_(6 7738972_67757489)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 67,474,434 | 67,501,350 | 67,738,972 | 67,757,489 |