nsv8357
- Organism: Homo sapiens
- Study:nstd4 (Perry et al. 2008)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:68,516
- Publication(s):Perry et al. 2008
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: 83 SVs from 13 studies. See in: genome view
Overlapping variant regions from other studies: 83 SVs from 13 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv8357 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 63,871,003 | 63,939,518 |
nsv8357 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 64,783,560 | 64,852,075 |
nsv8357 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 64,946,114 | 65,014,629 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv19737 | Remapped | Perfect | NC_000008.11:g.(63 871003_63934192)_( 63937963_63939518) del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 63,871,003 | 63,934,192 | 63,937,963 | 63,939,518 |
nssv19737 | Remapped | Perfect | NC_000008.10:g.(64 783560_64846749)_( 64850520_64852075) del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 64,783,560 | 64,846,749 | 64,850,520 | 64,852,075 |
nssv19737 | Submitted genomic | NC_000008.9:g.(649 46114_65009303)_(6 5013074_65014629)d el | NCBI35 (hg17) | NC_000008.9 | Chr8 | 64,946,114 | 65,009,303 | 65,013,074 | 65,014,629 |