nsv1238
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:63,719
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 283 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 283 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 28 SVs from 3 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv1238 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 34,748,141 | 34,811,859 |
nsv1238 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 35,217,347 | 35,281,065 |
nsv1238 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000014.7 | Chr14 | 34,287,098 | 34,350,816 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv4106 | Remapped | Perfect | NC_000014.9:g.(347 48141_?)_(?_347801 69)ins5014 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 34,748,141 | 34,780,169 |
nssv2917 | Remapped | Perfect | NC_000014.9:g.(347 78394_?)_(?_348118 59)ins6558 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 34,778,394 | 34,811,859 |
nssv4106 | Remapped | Perfect | NC_000014.8:g.(352 17347_?)_(?_352493 75)ins5014 | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 35,217,347 | 35,249,375 |
nssv2917 | Remapped | Perfect | NC_000014.8:g.(352 47600_?)_(?_352810 65)ins6558 | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 35,247,600 | 35,281,065 |
nssv4106 | Submitted genomic | NC_000014.7:g.(342 87098_?)_(?_343191 26)ins5014 | NCBI35 (hg17) | NC_000014.7 | Chr14 | 34,287,098 | 34,319,126 | ||
nssv2917 | Submitted genomic | NC_000014.7:g.(343 17351_?)_(?_343508 16)ins6558 | NCBI35 (hg17) | NC_000014.7 | Chr14 | 34,317,351 | 34,350,816 |