nsv3418736
- Organism: Homo sapiens
- Study:nstd162 (Audano et al. 2019)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:11
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Audano et al. 2019
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: 354 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 354 SVs from 34 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3418736 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nsv3418736 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv14752577 | insertion | SAMN09690649 | Sequencing | de novo and local sequence assembly | 21,495 |
nssv14757648 | insertion | SAMN02744161 | Sequencing | de novo and local sequence assembly | 20,941 |
nssv14760924 | insertion | SAMN05181962 | Sequencing | de novo and local sequence assembly | 23,563 |
nssv14762251 | insertion | SAMN05603847 | Sequencing | de novo and local sequence assembly | 26,021 |
nssv14762265 | insertion | SAMN03255769 | Sequencing | de novo and local sequence assembly | 21,134 |
nssv14762655 | insertion | SAMN06885952 | Sequencing | de novo and local sequence assembly | 28,070 |
nssv14762793 | insertion | SAMN05603729 | Sequencing | de novo and local sequence assembly | 24,108 |
nssv14764690 | insertion | SAMN04251426 | Sequencing | de novo and local sequence assembly | 22,074 |
nssv14766336 | insertion | SAMN04229548 | Sequencing | de novo and local sequence assembly | 23,009 |
nssv14768771 | insertion | SAMN09651199 | Sequencing | de novo and local sequence assembly | 27,381 |
nssv14771435 | insertion | SAMN09643900 | Sequencing | de novo and local sequence assembly | 26,631 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14752577 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14757648 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14760924 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14762251 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14762265 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14762655 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14762793 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14764690 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14766336 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14768771 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14771435 | Submitted genomic | NC_000008.11:g.150 8512_1508513ins648 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 1,508,512 | 1,508,512 | ||
nssv14752577 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14757648 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14760924 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14762251 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14762265 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14762655 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14762793 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14764690 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14766336 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14768771 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |
nssv14771435 | Remapped | Perfect | NC_000008.10:g.145 6678_1456679ins648 NC_000008.10:g.145 6678_1456679ins648 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 1,456,678 | 1,456,678 |