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nsv7058084

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,169

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 271 SVs from 43 studies. See in: genome view    
    Submitted genomic165,354,863-165,410,031Question Mark
    Overlapping variant regions from other studies: 271 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):166,276,015-166,331,183Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058084Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4165,354,863165,410,031
    nsv7058084RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4166,276,015166,331,183

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773148inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773148Submitted genomicNC_000004.12:g.165
    354863_165410031in
    v
    GRCh38 (hg38)NC_000004.12Chr4165,354,863165,410,031
    nssv18773148RemappedPerfectNC_000004.11:g.166
    276015_166331183in
    v
    GRCh37.p13First PassNC_000004.11Chr4166,276,015166,331,183

    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)
    nssv187731487e-062273814
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