nsv4415590
- 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:326,049
- DGV: gssvG6927
- dbVar: essv6996098
- dbVar: nssv1895607
- dbVar: nssv1895608
- dbVar: nssv1895609
- dbVar: nssv1895610
- dbVar: nssv1895611
- dbVar: nssv1895612
- dbVar: nssv1895613
- dbVar: nssv1895614
- dbVar: nssv1895615
- dbVar: nssv1895616
- dbVar: nssv3516015
- dbVar: nssv3710642
- dbVar: nssv3710643
- dbVar: nssv3710644
- dbVar: nssv3710645
- dbVar: nssv3710646
- dbVar: nssv3710647
- dbVar: nssv3710648
- dbVar: nssv3710649
- dbVar: nssv3710650
- dbVar: nssv3710651
- dbVar: nssv3710652
- dbVar: nssv3710653
- 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: 729 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 728 SVs from 71 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4415590 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 71,582,829 | 71,616,622 | 71,904,513 | 71,908,877 |
nsv4415590 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 71,293,875 | 71,327,668 | 71,615,559 | 71,619,923 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15708765 | copy number gain | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15708765 | Remapped | Perfect | NC_000011.10:g.(71 582829_71616622)_( 71904513_71908877) dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 71,582,829 | 71,616,622 | 71,904,513 | 71,908,877 |
nssv15708765 | Submitted genomic | NC_000011.9:g.(712 93875_71327668)_(7 1615559_71619923)d up | GRCh37 (hg19) | NC_000011.9 | Chr11 | 71,293,875 | 71,327,668 | 71,615,559 | 71,619,923 |