nsv470974
- Organism: Homo sapiens
- Study:nstd30 (Jakobsson et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:77,157
- Description:Single-copy duplication
- Publication(s):Jakobsson et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 730 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 730 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 373 SVs from 29 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 |
---|---|---|---|---|---|---|---|---|---|
nsv470974 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 131,049,527 | 131,126,683 |
nsv470974 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 132,847,790 | 132,924,946 |
nsv470974 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 132,737,780 | 132,814,936 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv545006 | Remapped | Perfect | NC_000010.11:g.(?_ 131049527)_(131126 683_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 131,049,527 | 131,126,683 |
nssv545007 | Remapped | Perfect | NC_000010.11:g.(?_ 131060995)_(131126 683_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 131,060,995 | 131,126,683 |
nssv545006 | Remapped | Perfect | NC_000010.10:g.(?_ 132847790)_(132924 946_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 132,847,790 | 132,924,946 |
nssv545007 | Remapped | Perfect | NC_000010.10:g.(?_ 132859258)_(132924 946_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 132,859,258 | 132,924,946 |
nssv545006 | Submitted genomic | NC_000010.9:g.(?_1 32737780)_(1328149 36_?)dup | NCBI36 (hg18) | NC_000010.9 | Chr10 | 132,737,780 | 132,814,936 | ||
nssv545007 | Submitted genomic | NC_000010.9:g.(?_1 32749248)_(1328149 36_?)dup | NCBI36 (hg18) | NC_000010.9 | Chr10 | 132,749,248 | 132,814,936 |