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nsv5492266

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,640

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 287 SVs from 47 studies. See in: genome view    
Submitted genomic80,112,988-80,135,627Question Mark
Overlapping variant regions from other studies: 287 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):81,872,744-81,895,383Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492266Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1080,112,98880,135,627
nsv5492266RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1081,872,74481,895,383

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037103duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037103Submitted genomicNC_000010.11:g.801
12988_80135627dup
GRCh38 (hg38)NC_000010.11Chr1080,112,98880,135,627
nssv17037103RemappedPerfectNC_000010.10:g.818
72744_81895383dup
GRCh37.p13First PassNC_000010.10Chr1081,872,74481,895,383

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17037103<0.00126404
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