nsv428155
- Organism: Homo sapiens
- Study:nstd8 (Perry et al. 2008b)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:20
- Validation:Not tested
- Clinical Assertions: No
- Region Size:142,483
- 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: 658 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 658 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 235 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv428155 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nsv428155 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nsv428155 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv450861 | copy number gain | HGDP00471 | BAC aCGH | Probe signal intensity | 73 |
| nssv450862 | copy number gain | HGDP00472 | BAC aCGH | Probe signal intensity | 65 |
| nssv450863 | copy number gain | HGDP00473 | BAC aCGH | Probe signal intensity | 64 |
| nssv450865 | copy number gain | HGDP00474 | BAC aCGH | Probe signal intensity | 56 |
| nssv450866 | copy number gain | HGDP00476 | BAC aCGH | Probe signal intensity | 69 |
| nssv450867 | copy number gain | HGDP00478 | BAC aCGH | Probe signal intensity | 38 |
| nssv450868 | copy number gain | HGDP00984 | BAC aCGH | Probe signal intensity | 75 |
| nssv450869 | copy number gain | HGDP00986 | BAC aCGH | Probe signal intensity | 82 |
| nssv450870 | copy number gain | HGDP01086 | BAC aCGH | Probe signal intensity | 52 |
| nssv450871 | copy number gain | HGDP01087 | BAC aCGH | Probe signal intensity | 75 |
| nssv450872 | copy number gain | HGDP01088 | BAC aCGH | Probe signal intensity | 78 |
| nssv450873 | copy number gain | HGDP01089 | BAC aCGH | Probe signal intensity | 65 |
| nssv450874 | copy number gain | HGDP01093 | BAC aCGH | Probe signal intensity | 95 |
| nssv450876 | copy number gain | HGDP01094 | BAC aCGH | Probe signal intensity | 92 |
| nssv450877 | copy number gain | NA18498 | BAC aCGH | Probe signal intensity | 97 |
| nssv450878 | copy number gain | NA19108 | BAC aCGH | Probe signal intensity | 84 |
| nssv450879 | copy number gain | NA19147 | BAC aCGH | Probe signal intensity | 75 |
| nssv450880 | copy number gain | NA19189 | BAC aCGH | Probe signal intensity | 94 |
| nssv450881 | copy number gain | NA19225 | BAC aCGH | Probe signal intensity | 71 |
| nssv450882 | copy number gain | NA19257 | BAC aCGH | Probe signal intensity | 86 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv450861 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450862 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450863 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450865 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450866 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450867 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450868 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450869 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450870 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450871 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450872 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450873 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450874 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450876 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450877 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450878 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450879 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450880 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450881 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450882 | Remapped | Perfect | NC_000006.12:g.(?_ 160516284)_(160658 766_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,516,284 | 160,658,766 |
| nssv450861 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450862 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450863 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450865 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450866 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450867 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450868 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450869 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450870 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450871 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450872 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450873 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450874 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450876 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450877 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450878 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450879 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450880 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450881 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450882 | Remapped | Perfect | NC_000006.11:g.(?_ 160937316)_(161079 798_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 160,937,316 | 161,079,798 |
| nssv450861 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450862 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450863 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450865 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450866 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450867 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450868 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450869 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450870 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450871 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450872 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450873 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450874 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450876 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450877 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450878 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450879 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450880 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450881 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 | ||
| nssv450882 | Submitted genomic | NC_000006.10:g.(?_ 160857306)_(160999 788_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,857,306 | 160,999,788 |