nsv498941
- Organism: Homo sapiens
- Study:nstd47 (Kidd et al. 2010b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:131,316
- Publication(s):Kidd 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: 690 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 690 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 301 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 | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv498941 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 152,810,211 | 152,941,526 |
nsv498941 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 153,666,725 | 153,798,040 |
nsv498941 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 153,374,971 | 153,506,286 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv585802 | copy number loss | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv585802 | Remapped | Perfect | NC_000002.12:g.152 810211_152941526de l | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 152,810,211 | 152,941,526 |
nssv585802 | Remapped | Perfect | NC_000002.11:g.153 666725_153798040de l | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 153,666,725 | 153,798,040 |
nssv585802 | Submitted genomic | NC_000002.10:g.153 374971_153506286de l | NCBI36 (hg18) | NC_000002.10 | Chr2 | 153,374,971 | 153,506,286 |