nsv820853
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,461
- Publication(s):Ju et al. 2010
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: 636 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 636 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 275 SVs from 22 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 |
---|---|---|---|---|---|---|---|---|---|
nsv820853 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 1,392,637 | 1,408,097 |
nsv820853 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_2 | Second Pass | NT_187654.1 | Chr8|NT_18 7654.1 | 2,921 | 18,381 |
nsv820853 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 1,340,803 | 1,356,263 |
nsv820853 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 1,328,210 | 1,343,670 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1420731 | Remapped | Perfect | NT_187654.1:g.(?_2 921)_(18381_?)del | GRCh38.p12 | Second Pass | NT_187654.1 | Chr8|NT_18 7654.1 | 2,921 | 18,381 |
nssv1420731 | Remapped | Perfect | NC_000008.11:g.(?_ 1392637)_(1408097_ ?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 1,392,637 | 1,408,097 |
nssv1420731 | Remapped | Perfect | NC_000008.10:g.(?_ 1340803)_(1356263_ ?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,340,803 | 1,356,263 |
nssv1420731 | Submitted genomic | NC_000008.9:g.(?_1 328210)_(1343670_? )del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 1,328,210 | 1,343,670 |