nsv442396
- Organism: Homo sapiens
- Study:nstd22 (McCarroll et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:37,411
- Publication(s):McCarroll 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: 357 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 226 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 10 SVs from 5 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 |
---|---|---|---|---|---|---|---|---|---|
nsv442396 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 35,787,547 | 35,824,957 |
nsv442396 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 35,021,918 | 35,059,328 |
nsv442396 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 34,879,419 | 34,916,829 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1660084 | Remapped | Perfect | NC_000016.10:g.(?_ 35787547)_(3582495 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,787,547 | 35,824,957 |
nssv1660085 | Remapped | Perfect | NC_000016.10:g.(?_ 35787547)_(3582495 7_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,787,547 | 35,824,957 |
nssv1660084 | Remapped | Perfect | NC_000016.9:g.(?_3 5021918)_(35059328 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 35,021,918 | 35,059,328 |
nssv1660085 | Remapped | Perfect | NC_000016.9:g.(?_3 5021918)_(35059328 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 35,021,918 | 35,059,328 |
nssv1660084 | Submitted genomic | NC_000016.8:g.(?_3 4879419)_(34916829 _?)dup | NCBI35 (hg17) | NC_000016.8 | Chr16 | 34,879,419 | 34,916,829 | ||
nssv1660085 | Submitted genomic | NC_000016.8:g.(?_3 4879419)_(34916829 _?)dup | NCBI35 (hg17) | NC_000016.8 | Chr16 | 34,879,419 | 34,916,829 |