nsv821007
- 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:34,025
- 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: 323 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 323 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 202 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 16 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 |
---|---|---|---|---|---|---|---|---|---|
nsv821007 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 85,506,792 | 85,540,816 |
nsv821007 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 85,972,475 | 86,006,499 |
nsv821007 | Remapped | Pass | GRCh37.p13 | PATCHES | Second Pass | NW_003871055.3 | Chr1|NW_00 3871055.3 | 2,338,129 | 2,368,708 |
nsv821007 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 85,745,063 | 85,779,087 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1420414 | Remapped | Perfect | NC_000001.11:g.(?_ 85506792)_(8554081 6_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 85,506,792 | 85,540,816 |
nssv1420414 | Remapped | Pass | NW_003871055.3:g.( ?_2338129)_(236870 8_?)dup | GRCh37.p13 | Second Pass | NW_003871055.3 | Chr1|NW_00 3871055.3 | 2,338,129 | 2,368,708 |
nssv1420414 | Remapped | Perfect | NC_000001.10:g.(?_ 85972475)_(8600649 9_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 85,972,475 | 86,006,499 |
nssv1420414 | Submitted genomic | NC_000001.9:g.(?_8 5745063)_(85779087 _?)dup | NCBI36 (hg18) | NC_000001.9 | Chr1 | 85,745,063 | 85,779,087 |