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nsv5484874

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,443

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Submitted genomic11,853,324-11,856,766Question Mark
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):11,895,323-11,898,765Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484874Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1011,853,32411,856,766
nsv5484874RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1011,895,32311,898,765

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17029191deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17029191Submitted genomicNC_000010.11:g.118
53324_11856766del
GRCh38 (hg38)NC_000010.11Chr1011,853,32411,856,766
nssv17029191RemappedPerfectNC_000010.10:g.118
95323_11898765del
GRCh37.p13First PassNC_000010.10Chr1011,895,32311,898,765

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)
nssv17029191<0.00116404
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