nsv4394401
- 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:515,380
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 2055 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 2055 SVs from 91 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4394401 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 56,049,407 | 56,065,649 | 56,447,155 | 56,564,786 |
nsv4394401 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 56,117,100 | 56,133,342 | 56,514,848 | 56,632,479 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15712489 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15712489 | Remapped | Perfect | NC_000007.14:g.(56 049407_56065649)_( 56447155_56564786) dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 56,049,407 | 56,065,649 | 56,447,155 | 56,564,786 |
nssv15712489 | Submitted genomic | NC_000007.13:g.(56 117100_56133342)_( 56514848_56632479) dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 56,117,100 | 56,133,342 | 56,514,848 | 56,632,479 |