nsv821156
- 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:17,792
- 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: 1820 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 1249 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 1820 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 1160 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 | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv821156 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 1,521,940 | 1,539,731 |
nsv821156 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 204,311 | 222,102 |
nsv821156 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 1,525,712 | 1,543,503 |
nsv821156 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 1,504,719 | 1,522,510 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1419937 | Remapped | Perfect | NT_187529.1:g.(?_2 04311)_(222102_?)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 204,311 | 222,102 |
nssv1419937 | Remapped | Perfect | NC_000002.12:g.(?_ 1521940)_(1539731_ ?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,521,940 | 1,539,731 |
nssv1419937 | Remapped | Perfect | NC_000002.11:g.(?_ 1525712)_(1543503_ ?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 1,525,712 | 1,543,503 |
nssv1419937 | Submitted genomic | NC_000002.10:g.(?_ 1504719)_(1522510_ ?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 1,504,719 | 1,522,510 |