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nsv3418736

  • Variant Calls:11
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 354 SVs from 34 studies. See in: genome view    
Submitted genomic1,508,512-1,508,512Question Mark
Overlapping variant regions from other studies: 354 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):1,456,678-1,456,678Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3418736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr81,508,5121,508,512
nsv3418736RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr81,456,6781,456,678

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14752577insertionSAMN09690649Sequencingde novo and local sequence assembly21,495
nssv14757648insertionSAMN02744161Sequencingde novo and local sequence assembly20,941
nssv14760924insertionSAMN05181962Sequencingde novo and local sequence assembly23,563
nssv14762251insertionSAMN05603847Sequencingde novo and local sequence assembly26,021
nssv14762265insertionSAMN03255769Sequencingde novo and local sequence assembly21,134
nssv14762655insertionSAMN06885952Sequencingde novo and local sequence assembly28,070
nssv14762793insertionSAMN05603729Sequencingde novo and local sequence assembly24,108
nssv14764690insertionSAMN04251426Sequencingde novo and local sequence assembly22,074
nssv14766336insertionSAMN04229548Sequencingde novo and local sequence assembly23,009
nssv14768771insertionSAMN09651199Sequencingde novo and local sequence assembly27,381
nssv14771435insertionSAMN09643900Sequencingde novo and local sequence assembly26,631

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14752577Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14757648Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14760924Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14762251Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14762265Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14762655Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14762793Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14764690Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14766336Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14768771Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14771435Submitted genomicNC_000008.11:g.150
8512_1508513ins648
GRCh38 (hg38)NC_000008.11Chr81,508,5121,508,512
nssv14752577RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14757648RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14760924RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14762251RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14762265RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14762655RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14762793RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14764690RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14766336RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14768771RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
nssv14771435RemappedPerfectNC_000008.10:g.145
6678_1456679ins648
NC_000008.10:g.145
6678_1456679ins648
GRCh37.p13First PassNC_000008.10Chr81,456,6781,456,678
Showing 22 of 33

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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