nsv8204
- Organism: Homo sapiens
- Study:nstd4 (Perry et al. 2008)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:63,912
- 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: 687 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 687 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|
nsv8204 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 111,454,424 | 111,518,335 |
nsv8204 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 111,094,480 | 111,158,391 |
nsv8204 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 110,688,431 | 110,752,342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv16588 | Remapped | Perfect | NC_000007.14:g.(11 1454424_111454953) _(111458047_111458 596)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 111,454,424 | 111,454,953 | 111,458,047 | 111,458,596 |
nssv14561 | Remapped | Perfect | NC_000007.14:g.(11 1456117_111456630) _(111517633_111518 335)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 111,456,117 | 111,456,630 | 111,517,633 | 111,518,335 |
nssv16588 | Remapped | Perfect | NC_000007.13:g.(11 1094480_111095009) _(111098103_111098 652)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 111,094,480 | 111,095,009 | 111,098,103 | 111,098,652 |
nssv14561 | Remapped | Perfect | NC_000007.13:g.(11 1096173_111096686) _(111157689_111158 391)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 111,096,173 | 111,096,686 | 111,157,689 | 111,158,391 |
nssv16588 | Submitted genomic | NC_000007.11:g.(11 0688431_110688960) _(110692054_110692 603)dup | NCBI35 (hg17) | NC_000007.11 | Chr7 | 110,688,431 | 110,688,960 | 110,692,054 | 110,692,603 | ||
nssv14561 | Submitted genomic | NC_000007.11:g.(11 0690124_110690637) _(110751640_110752 342)del | NCBI35 (hg17) | NC_000007.11 | Chr7 | 110,690,124 | 110,690,637 | 110,751,640 | 110,752,342 |