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nsv7054001

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,886

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
    Submitted genomic51,777,856-51,815,741Question Mark
    Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):51,811,872-51,849,757Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054001Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr351,777,85651,815,741
    nsv7054001RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr351,811,87251,849,757

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772351inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772351Submitted genomicNC_000003.12:g.517
    77856_51815741inv
    GRCh38 (hg38)NC_000003.12Chr351,777,85651,815,741
    nssv18772351RemappedPerfectNC_000003.11:g.518
    11872_51849757inv
    GRCh37.p13First PassNC_000003.11Chr351,811,87251,849,757

    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)
    nssv187723511.1e-053275014
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