nsv84871
- Organism: Homo sapiens
- Study:nstd6 (Mills et al. 2006)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,598
- Publication(s):Mills et al. 2006
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 127 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 127 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv84871 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 39,229,196 | 39,238,793 |
nsv84871 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 39,698,400 | 39,707,997 |
nsv84871 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000014.7 | Chr14 | 38,768,151 | 38,777,748 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv103449 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv103449 | Remapped | Perfect | NC_000014.9:g.3922 9196_39238793del95 98 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 39,229,196 | 39,238,793 |
nssv103449 | Remapped | Perfect | NC_000014.8:g.3969 8400_39707997del95 98 | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 39,698,400 | 39,707,997 |
nssv103449 | Submitted genomic | NC_000014.7:g.3876 8151_38777748del95 98 | NCBI35 (hg17) | NC_000014.7 | Chr14 | 38,768,151 | 38,777,748 |