nsv4360641
- Organism: Homo sapiens
- Study:nstd169 (Giner-Delgado et al. 2019)
- Variant Type:inversion
- Method Type:MLPA
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,096
- Publication(s):Giner-Delgado 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: 143 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 143 SVs from 45 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4360641 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 40,839,776 | 40,839,777 | 40,840,870 | 40,840,871 |
nsv4360641 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000007.13 | Chr7 | 40,879,375 | 40,879,376 | 40,880,469 | 40,880,470 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15607177 | inversion | MLPA | Genotyping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15607177 | Remapped | Perfect | NC_000007.14:g.(40 839776_40839777)_( 40840870_40840871) inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 40,839,776 | 40,839,777 | 40,840,870 | 40,840,871 |
nssv15607177 | Submitted genomic | NC_000007.13:g.(40 879375_40879376)_( 40880469_40880470) inv | GRCh37.p13 | NC_000007.13 | Chr7 | 40,879,375 | 40,879,376 | 40,880,469 | 40,880,470 |