nsv7386
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Yes
- Clinical Assertions: No
- Region Size:86,767
- Publication(s):Kidd et al. 2008
- TRACE: TEMPLATE_ID='1203737_ABC13_11_000049702400_B1'
- TRACE: TEMPLATE_ID='1203873_ABC13_11_000049765000_H21'
- TRACE: TEMPLATE_ID='1204935_ABC13_11_000047555400_N2'
- TRACE: TEMPLATE_ID='1204935_ABC13_11_000047627100_I16'
- TRACE: TEMPLATE_ID='1205403_ABC13_11_000047620300_E3'
- TRACE: TEMPLATE_ID='1205403_ABC13_11_000048902400_K13'
- 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: 353 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 353 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 10 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7386 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 141,845,467 | 141,932,233 |
| nsv7386 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 142,166,604 | 142,253,370 |
| nsv7386 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 142,208,297 | 142,295,063 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4945 | Remapped | Perfect | NC_000006.12:g.(14 1845467_?)_(?_1418 79622)inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 141,845,467 | 141,879,622 |
| nssv4946 | Remapped | Perfect | NC_000006.12:g.(14 1871585_?)_(?_1419 32233)inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 141,871,585 | 141,932,233 |
| nssv4945 | Remapped | Perfect | NC_000006.11:g.(14 2166604_?)_(?_1422 00759)inv | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 142,166,604 | 142,200,759 |
| nssv4946 | Remapped | Perfect | NC_000006.11:g.(14 2192722_?)_(?_1422 53370)inv | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 142,192,722 | 142,253,370 |
| nssv4945 | Submitted genomic | NC_000006.9:g.(142 208297_?)_(?_14224 2452)inv | NCBI35 (hg17) | NC_000006.9 | Chr6 | 142,208,297 | 142,242,452 | ||
| nssv4946 | Submitted genomic | NC_000006.9:g.(142 234415_?)_(?_14229 5063)inv | NCBI35 (hg17) | NC_000006.9 | Chr6 | 142,234,415 | 142,295,063 |